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

HEMOSTATIC/TUBE OCCLUDING FORCEPS

K Number: K800435 · Decision Mar 12, 1980
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
16
Review Days
14

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
HEMOSTATIC/TUBE OCCLUDING FORCEPS
K Number
K800435
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dravon Medical, Inc.
Date Received
February 27, 1980
Decision Date
March 12, 1980
Product Code
GEN
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEN Forceps, General & Plastic Surgery

Similar 510(k) Clearances

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

View all

Other Clearances by Dravon Medical, Inc.

K Number Device Name
K873455 S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSIS
K860770 AM-100 I/A AMPAC
K832739 STEDIFLO INFUSION SET
K831842 DRAVON T CLAMP
K812771 PERITONEAL DIALYSIS DRAINAGE
K812772 PERITONEAL DIALYSIS CYCLER SET (8UNIT)
K811851 S-610 SHUNT ADAPTOR SET
K782057 CATHETER, RADIOPAQUE TENCKHOFF
K782058 CATHETER, BETA-CAP-PERITONEAL
K781755 DAP-PAK
Search all 16 clearances from Dravon Medical, Inc. →