FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SINGLE-USE MINI-BULLDOG

K Number: K791098 · Decision Jun 22, 1979
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
12
Review Days
10

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
SINGLE-USE MINI-BULLDOG
K Number
K791098
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Med General
Date Received
June 12, 1979
Decision Date
June 22, 1979
Product Code
DXC
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DXC Clamp, Vascular

Similar 510(k) Clearances

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

View all

Other Clearances by Med General

K Number Device Name
K791097 CEPTORTRODE WITH CEPTOR HESIVE
K790763 MAXI-VAC TM
K790269 CEPTOR HESIVE
K782006 MEDGENERAL SINGLE-USE BULLDOG
K781239 MYO-STIM
K780632 MAXICEPTOR
K780698 STIMULATORS, NERVE, ELECTRICAL
K780117 CARDIOMETER
K771701 VESSEL-CLUDE
K771702 VESSEL-STABILIZER
Search all 12 clearances from Med General →