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

EN-BLOC BIOPSY SYSTEM, MODELS 777-110, 777-120, 770-001, 777002, 777-006, 777-301, 777-302

K Number: K020031 · Decision Mar 27, 2002
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
7
Review Days
82

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Basic Information

Device Name
EN-BLOC BIOPSY SYSTEM, MODELS 777-110, 777-120, 770-001, 777002, 777-006, 777-301, 777-302
K Number
K020031
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neothermia Corp.
Date Received
January 4, 2002
Decision Date
March 27, 2002
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 Neothermia Corp.

K Number Device Name
K041347 MODIFICATION TO EN-BLOC BIOPSY SYSTEM
K033427 MODIFICATION TO EN-BLOC BIOPSY SYSTEM
K023413 MODIFICATION TO NEOTHERMIA'S EN-BLOC BIOPSY SYSTEM
K022296 MODIFICATION TO EN-BLOC BIOPSY SYSTEM
K021577 MODIFICATION TO EN-BLOC BIOPSY SYSTEM
K003190 EN BLOC BIOPSY SYSTEM