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510(k) K911143

PB100 DIAGNOSTIC SPIROMETER by Puritan Bennett Corp. — Product Code BZM

K911143 is an FDA 510(k) premarket notification submitted by Puritan Bennett Corp. for the device "PB100 DIAGNOSTIC SPIROMETER". The FDA issued a decision of Substantially Equivalent on November 29, 1991. The device falls under product code BZM (Calculator, Pulmonary Function Interpretor (Diagnostic)), a Class II device regulated under 21 CFR 868.1900. Puritan Bennett Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 29, 1991
Date Received
March 14, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calculator, Pulmonary Function Interpretor (Diagnostic)
Device Class
Class II
Regulation Number
868.1900
Review Panel
AN
Submission Type

Other clearances by Puritan Bennett Corp.

  • K063650 — VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840 (February 15, 2007)
  • K053388 — MODEL 840 VENTILATOR WITH PROPORTIONAL ASSIST VENTILATION PLUS SOFTWARE OPTION (April 4, 2006)
  • K023225 — PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWARE (December 18, 2002)
  • K022103 — PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM (September 27, 2002)
  • K001646 — PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTION (October 20, 2000)
  • K002001 — BREEZE SLEEPGEAR WITH DREAMSEAL (September 6, 2000)
  • K993071 — PURITAN-BENNETT VENTILATOR SYSTEM WITH ET/TRACHEOSTOMY TUBE COMPENSATION, TC, OP (November 24, 1999)
  • K993220 — PURITAN-BENNETT HELIOS PORTABLE LIQUID OXYGEN SYSTEM (October 22, 1999)
  • K993088 — PURITAN-BENNETT AERIS 590 OXYGEN CONCENTRATOR WITH OCI (October 8, 1999)
  • K984535 — PURITAN-BENNETT 840 VENTILATORY SYSTEM WITH BILEVEL OPTION (December 28, 1998)

Other clearances for product code BZM

  • K102229 — PULMOTRACK 2020 SYSTEM (March 4, 2011)
  • K090863 — PERSONAL WHEEZOMETER (September 21, 2009)
  • K071955 — WIM-PC, MODEL 1010 (November 1, 2007)
  • K012387 — STG MULTICHANNEL LUNG SOUND ANALYSIS SYSTEM (April 23, 2002)
  • K980878 — PULMOTRACK,MODEL 1010 (December 28, 1998)
  • K974200 — ORCA CARDIOPULMONARY EXERCISE TESTING SYSTEM (July 21, 1998)
  • K955432 — CPX, CCM, CATH WITH 15% CO2 (July 1, 1996)
  • K923209 — MEDGRAPHICS EXERCISE CONSULT (March 11, 1993)
  • K896345 — EXERCISE EVALUATION SYSTEM 2010 (January 20, 1990)
  • K880550 — BURROWS-KNUDSON AUTOMATED LUNG FUNCTION INTER. SYS (July 25, 1988)

FDA data resources