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

INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE

K Number: K882421 · Decision Jun 30, 1988
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
35
Applicant Total
8
Review Days
17

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Basic Information

Device Name
INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE
K Number
K882421
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
June 13, 1988
Decision Date
June 30, 1988
Product Code
JOS
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
JOS Electrode, Electrosurgical

Similar 510(k) Clearances

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Other Clearances by Dermacare Products, Inc.

K Number Device Name
K882494 ELAN-E DISPOSALBE DRAPE
K871910 SURGITEK DISPOSABLE BIPOLAR CORD
K863279 SURGI-TEK TUBE POSITIONER
K863280 DERMAMARKER
K863278 SURGI-WIPES
K862367 PRO-CLEAN
K853374 CORRECT-A-COUNT