510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K962903Substantially Equivalent

Prestige Medical Series 2100 Clinical Autoclave

Prestige Medical, Ltd., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K962903 is the FDA 510(k) clearance record for PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE, a class II device, cleared for Prestige Medical Corp. on under FDA product code FLE (Sterilizer, Steam). FDA records list one 510(k) clearance for Prestige Medical Corp. As of , FDA records show no recalls naming K962903.

Clearance record

Decision date
Received
(586 days to decision)
Product code
FLE Sterilizer, Steam
Regulation
21 CFR 880.6880
Device class
Class II
Review panel
General Hospital
Applicant
Prestige Medical Corp. 1455 Pennsylvania Ave., NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code FLE

Trailing 12 months
4 clearances under product code FLE in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FLE, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20261
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260