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

SAFTI-BRACELET

K Number: K853418 · Decision Sep 20, 1985
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
63
Applicant Total
22
Review Days
37

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
SAFTI-BRACELET
K Number
K853418
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5210
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Advanced Biosearch Assn.
Date Received
August 14, 1985
Decision Date
September 20, 1985
Product Code
KMK
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KMK Device, Intravascular Catheter Securement

Similar 510(k) Clearances

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

View all

Other Clearances by Advanced Biosearch Assn.

K Number Device Name
K905514 AUTOGENESIS(TM) AUTOMATOR
K883888 CATHSCANNER INTRAVASCULAR ULTRASONIC IMAGING SYST.
K854770 MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM
K855030 CHAMPY BONE PLATES & BONE SCREWS
K855031 MANUAL SURGICAL INSTRUMENTS & ACCESS.CHAMPY BONE P
K853916 P.M. HIP-FEMORAL PROSTHESIS
K852839 FREEMAN HIP
K852517 CLS HIP PROSTHESIS
K852699 FREEMAN ACETABULAR CUP
K850773 PM CEMENTLESS SCREW-IN ACETABULAR CUP
Search all 22 clearances from Advanced Biosearch Assn. →