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

COPAN VENTURI TRANSYSTEM STUARTS MEDIUM

K Number: K946285 · Decision Mar 10, 1995
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
110
Applicant Total
10
Review Days
73

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
COPAN VENTURI TRANSYSTEM STUARTS MEDIUM
K Number
K946285
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2390
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Copan Diagnostics, Inc.
Date Received
December 27, 1994
Decision Date
March 10, 1995
Product Code
JSM
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
JSM Culture Media, Non-Propagating Transport

Similar 510(k) Clearances

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

View all

Other Clearances by Copan Diagnostics, Inc.

K Number Device Name
K061301 COPAN LIQUID AMIES ELUTION SWAB (ESWAB) COLLECTION AND TRANSPORT SYSTEM
K042970 COPAN UNIVERSAL TRANSPORT MEDIUM (UTM-RT) SYSTEM
K001780 COPAN VIRAL TRANSYSTEM
K993161 COPAN EASY-SWAB COLLECTION AND TRANSPORT SYSTEM
K946283 COPAN VENTURI TRANSYSTEM LIQUID STUARTS MEDIUM
K946287 COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITHOUT CHARCOAL
K946286 COPAN VENTURI TRANSYSTEM CARY-BLAIR MEDIUM
K946288 COPAN VENTURI TRANSYSTEM LIQUID AMIES MEDIUM
K946284 COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL