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

SAFETY VEST

K Number: K962429 · Decision Sep 18, 1996
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
133
Applicant Total
206
Review Days
86

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Basic Information

Device Name
SAFETY VEST
K Number
K962429
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6760
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Johnson & Johnson Professionals, Inc.
Date Received
June 24, 1996
Decision Date
September 18, 1996
Product Code
FMQ
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
FMQ Restraint, Protective

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K982379 SUNDT SLIM-LINE ANEURYSM CLIP APPLIER
K982812 G2 TOTAL HIP SYSTEM FEMORAL STEM (11/13 TAPER)
K983141 CAPITELLO-CONDYLAR TOTAL ELBOW PROSTHESIS
K983014 SUMMIT ACETABULAR SYSTEM
K980778 HAKIM MICRO PROGRAMMABLE VALVE SYSTEM
K974739 HAKIM PROGRAMMABLE VALVE SYSTEM
K980801 J-FX BIPOLAR HEAD
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