510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781727Substantially Equivalent

Change in Sterilization Procedure

Absorbent Cotton Co., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K781727 is the FDA 510(k) clearance record for CHANGE IN STERILIZATION PROCEDURE, a class I device, cleared for Absorbent Cotton Co., Inc. on under FDA product code GOY (Antisera, Agglutinating, B. Pertussis, All). FDA records list 10 510(k) clearances for Absorbent Cotton Co., Inc., from to . As of , FDA records show no recalls naming K781727.

Clearance record

Decision date
Received
(54 days to decision)
Product code
GOY Antisera, Agglutinating, B. Pertussis, All
Regulation
21 CFR 866.3065
Device class
Class I
Review panel
Microbiology
Applicant
Absorbent Cotton Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GOY

Trailing 12 months

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

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