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

SURGICAL BURS

K Number: K880706 · Decision Feb 26, 1988
Classifications
1
FEI Numbers
178
Registration Numbers
178
Same Product Code
15
Applicant Total
3
Review Days
4

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Basic Information

Device Name
SURGICAL BURS
K Number
K880706
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Nuell Air Equipment & Hospital Supplies, Inc.
Date Received
February 22, 1988
Decision Date
February 26, 1988
Product Code
GFF
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
GFF Bur, Surgical, General & Plastic Surgery

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Other Clearances by Nuell Air Equipment & Hospital Supplies, Inc.

K Number Device Name
K881418 CRANIOTOME BLADE OR NEURO BLADE
K880601 WIRE PASS DRILL BITS