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

NDM DIATEMP INFANT ELECTROSURG. DISP. P.

K Number: K810920 · Decision May 1, 1981
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
30
Applicant Total
11
Review Days
25

Basic Information

Device Name
NDM DIATEMP INFANT ELECTROSURG. DISP. P.
K Number
K810920
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
NDM CORP.
Date Received
April 6, 1981
Decision Date
May 1, 1981
Product Code
HAM
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
HAM Apparatus, Electrosurgical

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