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510(k) K914896

FRIEDMANN ANALYSER 3 by Clement Clarke, Inc. — Product Code HOK

K914896 is an FDA 510(k) premarket notification submitted by Clement Clarke, Inc. for the device "FRIEDMANN ANALYSER 3". The FDA issued a decision of Substantially Equivalent on January 23, 1992. The device falls under product code HOK (Screen, Tangent, Projection, Ac-Powered), a Class I device regulated under 21 CFR 886.1810. Clement Clarke, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 23, 1992
Date Received
October 31, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Screen, Tangent, Projection, Ac-Powered
Device Class
Class I
Regulation Number
886.1810
Review Panel
OP
Submission Type

Other clearances by Clement Clarke, Inc.

  • K961512 — PERKINS HAND-HELD APPLANATION TONOMETER (July 18, 1996)
  • K952713 — MINI WRIGHT LR AFS (March 29, 1996)
  • K953965 — 904 SLIT LAMP (September 27, 1995)
  • K932258 — OPTICOM M600 (July 25, 1994)
  • K914126 — VMX MINI-LOG FLOWMETER (March 5, 1993)
  • K912397 — PROFESSIONAL INDIRECT OPHTHALMOSCOPE (October 23, 1991)
  • K895953 — WRIGHT VENTILOMETER VM-1 (February 2, 1990)
  • K841430 — LASERSPEC (December 13, 1984)
  • K781313 — VISION-STIMULATOR, CAM (January 26, 1979)

FDA data resources