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

ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100

K Number: K852683 · Decision Aug 12, 1985
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
59
Review Days
48

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Basic Information

Device Name
ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100
K Number
K852683
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
American Bentley
Date Received
June 25, 1985
Decision Date
August 12, 1985
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

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K870804 CARDIOPLEGIA HEAT EXCHANGER MODEL NO. HE-100
K872133 OXYGENATOR MODEL NO. BENTLEY 5 PLUS
K870911 INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY
K870269 ELECTROSURGICAL MENISCUS CUTTER (EMC) MOD. AMC-100
K863249 OXYGENATOR MODEL NO. BENTLEY-10 PLUS
K861641 HEPARIN-COATED EXTRACORPOREAL CIRCUITS
K862549 ARTERIAL BLOOD FILTER HOLDER MODEL NO. AF-HE
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