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

BERNSCO NEEDLE ADAPTER

K Number: K883774 · Decision Oct 4, 1988
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
4
Review Days
28

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Basic Information

Device Name
BERNSCO NEEDLE ADAPTER
K Number
K883774
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Bernsco Surgical Supply, Inc.
Date Received
September 6, 1988
Decision Date
October 4, 1988
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

Other 510(k) clearances with the same product code (GEI), ordered by most recent decision date.

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Other Clearances by Bernsco Surgical Supply, Inc.

K Number Device Name
K922999 SEGAL REUSABLE ELECTRODE
K900629 BERNSCO LUER NEEDLER ADAPTOR
K883823 BERNSCO ELECTROSURGICAL SHIELD