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510(k) K863953

SPIROMETRICS MODEL 2500 FLOWMATE(TM) by Spirometrics, Inc. — Product Code BZM

K863953 is an FDA 510(k) premarket notification submitted by Spirometrics, Inc. for the device "SPIROMETRICS MODEL 2500 FLOWMATE(TM)". The FDA issued a decision of Substantially Equivalent on January 15, 1987. The device falls under product code BZM (Calculator, Pulmonary Function Interpretor (Diagnostic)), a Class II device regulated under 21 CFR 868.1900. Spirometrics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 15, 1987
Date Received
October 10, 1986
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 Spirometrics, Inc.

  • K915059 — PEAK FLOW MONITOR (July 27, 1992)
  • K911358 — CMD/DLCO DIAGNOSTIC SPIROMETER (July 22, 1991)
  • K900322 — CO/CMD-1 (April 30, 1990)
  • K900673 — SERIAL FLOW (April 3, 1990)
  • K901057 — SPIROMETRICS MODEL 2600 MIRO SPIROMETER (April 3, 1990)
  • K884464 — SPIROMETRICS MODEL 2200 SM200 FLOW SENSOR (January 19, 1989)
  • K884465 — SPIROMETRICS MODEL 2141 SPIRO-FILTER(TM) (November 9, 1988)
  • K850045 — SPIROMETRICS 2453 & SMI III (February 14, 1985)
  • K844333 — SPIROMETRICS 2451 & SMI I (November 20, 1984)
  • K831497 — SPIROMETRICS BREON 2400 & SMI 2400 (June 24, 1983)

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)
  • K911143 — PB100 DIAGNOSTIC SPIROMETER (November 29, 1991)
  • K896345 — EXERCISE EVALUATION SYSTEM 2010 (January 20, 1990)

FDA data resources