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510(k) K841430

LASERSPEC by Clement Clarke, Inc.

K841430 is an FDA 510(k) premarket notification submitted by Clement Clarke, Inc. for the device "LASERSPEC". The FDA issued a decision of Substantially Equivalent on December 13, 1984. Clement Clarke, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 13, 1984
Date Received
April 6, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

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)
  • K914896 — FRIEDMANN ANALYSER 3 (January 23, 1992)
  • K912397 — PROFESSIONAL INDIRECT OPHTHALMOSCOPE (October 23, 1991)
  • K895953 — WRIGHT VENTILOMETER VM-1 (February 2, 1990)
  • K781313 — VISION-STIMULATOR, CAM (January 26, 1979)

FDA data resources