FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

HEMOSTASYL PASTE

K Number: K082116 · Decision Dec 17, 2008
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
35
Applicant Total
24
Review Days
142

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
HEMOSTASYL PASTE
K Number
K082116
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Satelec
Date Received
July 28, 2008
Decision Date
December 17, 2008
Product Code
MVL
Advisory Committee
Unknown
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
MVL Cord, Retraction

Similar 510(k) Clearances

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

View all

Other Clearances by Satelec

K Number Device Name
K110379 AIR-N-GO
K100410 PIEZOELECTRIC SYSTEM
K091331 PIEZOTOME 2
K091252 IMPLANT CENTER 2
K072181 MINI LED AUTOFOCUS
K071965 I-SURGE
K060275 PIEZOTOME
K060274 PIEZOTOME
K053328 BIOSPLINT SPLINTING RIBBON
K050895 SURPASSON P5 NEWTRON
Search all 24 clearances from Satelec →