510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830276Substantially Equivalent

Securet Drape & Instrument Retainer/incl

Ritmed, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830276 is the FDA 510(k) clearance record for SECURET DRAPE & INSTRUMENT RETAINER/INCL, a class I device, cleared for Ritmed, Inc. on under FDA product code GTC (Antisera, All Types, Klebsiella Spp.). FDA records list 22 510(k) clearances for Ritmed, Inc., from to . As of , FDA records show no recalls naming K830276.

Clearance record

Decision date
Received
(63 days to decision)
Product code
GTC Antisera, All Types, Klebsiella Spp.
Regulation
21 CFR 866.3340
Device class
Class I
Review panel
Microbiology
Applicant
Ritmed, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GTC

Trailing 12 months

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

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