510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K831722Substantially Equivalent

Ac-22 Autoclave Tape

Armak Tape Division, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831722 is the FDA 510(k) clearance record for AC-22 AUTOCLAVE TAPE, a class II device, cleared for Armak Tape Division on under FDA product code JOJ (Indicator, Physical/Chemical Sterilization Process). FDA records list one 510(k) clearance for Armak Tape Division. As of , FDA records show no recalls naming K831722.

Clearance record

Decision date
Received
(36 days to decision)
Product code
JOJ Indicator, Physical/Chemical Sterilization Process
Regulation
21 CFR 880.2800
Device class
Class II
Review panel
General Hospital
Applicant
Armak Tape Division 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JOJ

Trailing 12 months
3 clearances under product code JOJ 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 JOJ, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260