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

H.R. JAKOBI SURG. INSTRU. SECT. 48

K Number: K834542 · Decision Jan 27, 1984
Classifications
1
FEI Numbers
653
Registration Numbers
653
Same Product Code
72
Applicant Total
52
Review Days
67

Basic Information

Device Name
H.R. JAKOBI SURG. INSTRU. SECT. 48
K Number
K834542
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
IMM ENTERPRISES LTD.
Date Received
November 21, 1983
Decision Date
January 27, 1984
Product Code
HTD
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
HTD Forceps

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