510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K993535Substantially Equivalent

Metapak Multi-Purpose Instrument Tray

Riley Medical, Inc., North Attleboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K993535 is the FDA 510(k) clearance record for METAPAK MULTI-PURPOSE INSTRUMENT TRAY, a class II device, cleared for Riley Medical, Inc. on under FDA product code FRG (Wrap, Sterilization). FDA records list 2 510(k) clearances for Riley Medical, Inc., from to . As of , FDA records show no recalls naming K993535.

Clearance record

Decision date
Received
(780 days to decision)
Product code
FRG Wrap, Sterilization
Regulation
21 CFR 880.6850
Device class
Class II
Review panel
General Hospital
Applicant
Riley Medical, Inc. 49 Plain St., North Attleboro MA
510(k) summary
Summary
Third party review
No

Clearances, product code FRG

Trailing 12 months
5 clearances under product code FRG in the twelve months to October 2026, May 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FRG, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20262
June 20260
July 20261
August 20260
September 20260
October 20260