Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K972138Substantially Equivalent

Carr Rigid Container System

Carr Metal Products, Inc., Indianapolis IN / Traditional, Substantially Equivalent

K972138 is the FDA 510(k) clearance record for CARR RIGID CONTAINER SYSTEM, a class II device, cleared for Carr Metal Products, Inc. on under FDA product code FRG (Wrap, Sterilization). FDA records list 2 510(k) clearances for Carr Metal Products, Inc., from to . As of , FDA records show no recalls naming K972138.

Clearance record

Decision date
Received
(160 days to decision)
Product code
FRG Wrap, Sterilization
Regulation
21 CFR 880.6850
Device class
Class II
Review panel
General Hospital
Applicant
Carr Metal Products, Inc. 3735 N. Arlington Ave., Indianapolis IN
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