510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K851238Substantially Equivalent

Chamber V-9 Plus Agar

Bug City Company, Inc., Sapulpa OK / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K851238 is the FDA 510(k) clearance record for CHAMBER V-9 PLUS AGAR, a class I device, cleared for Bug City Company, Inc. on under FDA product code JSJ (Culture Media, Selective And Non-Differential). FDA records list one 510(k) clearance for Bug City Company, Inc. As of , FDA records show no recalls naming K851238.

Clearance record

Decision date
Received
(63 days to decision)
Product code
JSJ Culture Media, Selective And Non-Differential
Regulation
21 CFR 866.2360
Device class
Class I
Review panel
Microbiology
Applicant
Bug City Company, Inc. Bartlett Memorial Center Inc., Sapulpa OK
Third party review
No

Clearances, product code JSJ

Trailing 12 months

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

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