510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920883Substantially Equivalent

Hemostat, Surgical (Various Types)

S.T.S Instruments, Brooklyn NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920883 is the FDA 510(k) clearance record for HEMOSTAT, SURGICAL (VARIOUS TYPES), a class I device, cleared for S.T.S Instruments on under FDA product code EMD (Hemostat, Surgical). FDA records list one 510(k) clearance for S.T.S Instruments. As of , FDA records show no recalls naming K920883.

Clearance record

Decision date
Received
(16 days to decision)
Product code
EMD Hemostat, Surgical
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
S.T.S Instruments 766 E. 9th St., Brooklyn NY
510(k) summary
Statement
Third party review
No

Clearances, product code EMD

Trailing 12 months

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

FDA records show no clearances under product code EMD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EMD, 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