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
K871238Substantially Equivalent

Anabag

Scott Laboratories, Inc., Fiskeville RI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871238 is the FDA 510(k) clearance record for ANABAG, a class I device, cleared for Scott Laboratories, Inc. on under FDA product code KZJ (Device, Gas Generating). FDA records list 16 510(k) clearances for Scott Laboratories, Inc., from to . As of , FDA records show no recalls naming K871238.

Clearance record

Decision date
Received
(7 days to decision)
Product code
KZJ Device, Gas Generating
Regulation
21 CFR 866.2580
Device class
Class I
Review panel
Microbiology
Applicant
Scott Laboratories, Inc.
Third party review
No

Clearances, product code KZJ

Trailing 12 months

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

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