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

SURGITEK DISPOSABLE BIPOLAR CORD

K Number: K871910 · Decision Jun 1, 1987
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
8
Review Days
14

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Basic Information

Device Name
SURGITEK DISPOSABLE BIPOLAR CORD
K Number
K871910
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dermacare Products, Inc.
Date Received
May 18, 1987
Decision Date
June 1, 1987
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

Similar 510(k) Clearances

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Other Clearances by Dermacare Products, Inc.

K Number Device Name
K882494 ELAN-E DISPOSALBE DRAPE
K882421 INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE
K863279 SURGI-TEK TUBE POSITIONER
K863280 DERMAMARKER
K863278 SURGI-WIPES
K862367 PRO-CLEAN
K853374 CORRECT-A-COUNT