510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K834558Substantially Equivalent

Ck10000 Series Pouch & Bags Etc.

Currie Medical Specialties, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K834558 is the FDA 510(k) clearance record for CK10000 SERIES POUCH & BAGS ETC., a class II device, cleared for Currie Medical Specialties, Inc. on under FDA product code KCT (Sterilization Wrap Containers, Trays, Cassettes & Other Accessories). FDA records list 13 510(k) clearances for Currie Medical Specialties, Inc., from to . As of , FDA records show no recalls naming K834558.

Clearance record

Decision date
Received
(252 days to decision)
Product code
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Regulation
21 CFR 880.6850
Device class
Class II
Review panel
General Hospital
Applicant
Currie Medical Specialties, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code KCT

Trailing 12 months
8 clearances under product code KCT in the twelve months to October 2026, June 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code KCT, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20262
March 20260
April 20260
May 20260
June 20263
July 20260
August 20260
September 20262
October 20260