FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

V AGAR

K Number: K850844 · Decision Mar 20, 1985
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
145
Applicant Total
52
Review Days
19

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
V AGAR
K Number
K850844
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2320
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Micro Media Laboratories
Date Received
March 1, 1985
Decision Date
March 20, 1985
Product Code
JSH
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JSH Culture Media, Non-Selective And Differential

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JSH), ordered by most recent decision date.

View all

Other Clearances by Micro Media Laboratories

K Number Device Name
K853691 TERGITOL 7 AGAR
K853690 COLUMBIZ BLOOD AGAR
K851344 OXIDATIVE FORMENTIVE MEDIUM
K851343 BROM CRESOL PURPLE STARCH
K851348 COBA AGAR
K851347 KANAMYCIN-VANCOMYCIN-LAKED BLOOD AGAR
K851345 PURPLE BROTH
K851346 PHENYLALANINE AGAR
K850848 BRAIN HEART INFUSION AGAR
K850846 SALT BROTH
Search all 52 clearances from Micro Media Laboratories →