510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K831592Substantially Equivalent

Anhydric Incubators, Culture Incubator

Boekel Industries, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831592 is the FDA 510(k) clearance record for ANHYDRIC INCUBATORS, CULTURE INCUBATOR, a class I device, cleared for Boekel Industries, Inc. on under FDA product code JTQ (Bath, Incubators/Water, All). FDA records list 3 510(k) clearances for Boekel Industries, Inc., from to . As of , FDA records show no recalls naming K831592.

Clearance record

Decision date
Received
(30 days to decision)
Product code
JTQ Bath, Incubators/Water, All
Regulation
21 CFR 866.2540
Device class
Class I
Review panel
Microbiology
Applicant
Boekel Industries, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JTQ

Trailing 12 months

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

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