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

HERPES TRANSETTE

K Number: K823443 · Decision Dec 3, 1982
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
42
Applicant Total
3
Review Days
17

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
HERPES TRANSETTE
K Number
K823443
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2900
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Spectrum Diagnostic, Inc.
Date Received
November 16, 1982
Decision Date
December 3, 1982
Product Code
JTW
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
JTW System, Transport, Aerobic

Similar 510(k) Clearances

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

View all

Other Clearances by Spectrum Diagnostic, Inc.

K Number Device Name
K831579 GONORRHEA TRANSETTE 1 & 3
K822886 GONORRHEA TRANSETTE 3