Home / 510(k) Clearances / K983551

510(k) K983551

CRIT-SCAN II MONITOR by In-Line Diagnostics Corp. — Product Code GKF

K983551 is an FDA 510(k) premarket notification submitted by In-Line Diagnostics Corp. for the device "CRIT-SCAN II MONITOR". The FDA issued a decision of Substantially Equivalent on May 27, 1999. The device falls under product code GKF (Instrument, Hematocrit, Automated), a Class II device regulated under 21 CFR 864.5600. In-Line Diagnostics Corp. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 27, 1999
Date Received
October 9, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Hematocrit, Automated
Device Class
Class II
Regulation Number
864.5600
Review Panel
HE
Submission Type

Other clearances by In-Line Diagnostics Corp.

  • K001763 — CRIT-LINE MONITOR III (CLM III) (December 20, 2000)
  • K992227 — CRIT-LINE MONITOR III (CLM III) (July 30, 1999)
  • K982412 — MODIFICATION OF CRIT-LINE MONITOR III (CLM III) (October 9, 1998)
  • K972470 — CRIT-LINE MONITOR (CLMIII) (December 11, 1997)
  • K953875 — CRIT-LINE HEMATOCRIT ALERT (MODIFICATION) (July 23, 1996)
  • K950942 — CRIT-LINE HEMATOCRIT ALERT (March 14, 1995)
  • K935958 — CRIT-LINE BLOOD CHAMBER WITH E-BEAM (January 19, 1995)

Other clearances for product code GKF

  • K160415 — GEM Premier 5000 (Measured parameters: Hematocrit, Total Hemoglobin, Carboxyhemo (December 14, 2016)
  • K981427 — STAT PROFILE M ANALYZER (May 12, 1998)
  • K981426 — STAT PROFILE ULTRA F,G,H,I,J,K, AND L ANALYZERS (May 12, 1998)
  • K981425 — STAT PROFILE ULTRA A, B, C, D, AND E ANALYZERS (May 12, 1998)
  • K953519 — MICROSPIN 24 (November 3, 1995)
  • K915825 — MARATHON 6K GENERAL-PURPOSE CENTRIFUGE (March 11, 1992)
  • K915441 — MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE (January 8, 1992)
  • K904336 — NEW COBE SATURATION/HEMATOCRIT MONITOR (December 27, 1990)
  • K880373 — IONOMETER E-HK AND ACCESSORIES (March 17, 1988)
  • K870860 — CHEMPRO 1000(TM) (April 14, 1987)

FDA data resources