510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K896296Substantially Equivalent

Inpouch-Tv Pouch

Biomed Diagnostics, Inc., San Jose CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896296 is the FDA 510(k) clearance record for INPOUCH-TV POUCH, a class I device, cleared for Biomed Diagnostics, Inc. on under FDA product code JSN (Culture Media, Propagating Transport). FDA records list 2 510(k) clearances for Biomed Diagnostics, Inc., from to . As of , FDA records show no recalls naming K896296.

Clearance record

Decision date
Received
(90 days to decision)
Product code
JSN Culture Media, Propagating Transport
Regulation
21 CFR 866.2390
Device class
Class I
Review panel
Microbiology
Applicant
Biomed Diagnostics, Inc. 810 Menkar Ave., San Jose CA
Third party review
No

Clearances, product code JSN

Trailing 12 months

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

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