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

REUSABLE HAND-TROL

K Number: K800597 · Decision Apr 2, 1980
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
55
Review Days
16

Basic Information

Device Name
REUSABLE HAND-TROL
K Number
K800597
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
ASPEN LABORATORIES, INC.
Date Received
March 17, 1980
Decision Date
April 2, 1980
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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