510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K260181Substantially Equivalent

LF Process Indicator Tape for Steam Sterilization

Intertape Polymer Group, Sarasota FL / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K260181 is the FDA 510(k) clearance record for LF Process Indicator Tape for Steam Sterilization, a class II device, cleared for Intertape Polymer Group on under FDA product code JOJ (Indicator, Physical/Chemical Sterilization Process). FDA records list one 510(k) clearance for Intertape Polymer Group. As of , FDA records show no recalls naming K260181.

Clearance record

Decision date
Received
(30 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
Intertape Polymer Group 100 Paramount Dr., Sarasota FL
510(k) summary
Summary PDF
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