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

THE ON-GARD CORD-CADDY

K Number: K903855 · Decision Sep 7, 1990
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
2
Review Days
17

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Basic Information

Device Name
THE ON-GARD CORD-CADDY
K Number
K903855
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
On-Gard Systems, Inc.
Date Received
August 21, 1990
Decision Date
September 7, 1990
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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Other Clearances by On-Gard Systems, Inc.

K Number Device Name
K895220 THE ON-GARD RECAPPER