510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873554Substantially Equivalent

Gorsk Instrument Rest

Gorsk, Inc., Camarillo CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873554 is the FDA 510(k) clearance record for GORSK INSTRUMENT REST, a class I device, cleared for Gorsk, Inc. on under FDA product code HMG (Stand, Instrument, Ophthalmic, Non-Powered). FDA records list 2 510(k) clearances for Gorsk, Inc. As of , FDA records show no recalls naming K873554.

Clearance record

Decision date
Received
(56 days to decision)
Product code
HMG Stand, Instrument, Ophthalmic, Non-Powered
Regulation
21 CFR 886.1860
Device class
Class I
Review panel
Ophthalmic
Applicant
Gorsk, Inc. P.O. Box 398, Camarillo CA
Third party review
No

Clearances, product code HMG

Trailing 12 months

FDA records hold no clearances under product code HMG in the trailing twelve months.

FDA records show no clearances under product code HMG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HMG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260