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

CAUTERIES, HOT WIRE, DISP.

K Number: K772199 · Decision Dec 13, 1977
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
211
Review Days
13

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Basic Information

Device Name
CAUTERIES, HOT WIRE, DISP.
K Number
K772199
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Intermedics, Inc.
Date Received
November 30, 1977
Decision Date
December 13, 1977
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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Other Clearances by Intermedics, Inc.

K Number Device Name
K954610 MODEL 430-07 ENDOCARDIAL PACING LEAD
K955122 INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD
K962174 BIPLR IM EN PAC LEADS (430-07,432-03,436-02 & 07, 438-05 & 07)
K955550 CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD
K960281 IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORY
K954719 INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD
K933278 INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04
K922042 CARDIFIX ENDOCARDIAL PACING LEAD
K922972 MODELS 438-05 AND 435-05 IMPLANTABLE PACING LEAD
K920530 INTERMEDICS MODEL 366-15 VS 1 HEADER PLUG
Search all 211 clearances from Intermedics, Inc. →