FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

COPE LUNG FORCEPS #305-218

K Number: K771624 · Decision Sep 6, 1977
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
11
Review Days
12

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Basic Information

Device Name
COPE LUNG FORCEPS #305-218
K Number
K771624
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
J. Jamner Surgical Instruments, Inc.
Date Received
August 25, 1977
Decision Date
September 6, 1977
Product Code
GEN
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
GEN Forceps, General & Plastic Surgery

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Other Clearances by J. Jamner Surgical Instruments, Inc.

K Number Device Name
K082349 JARIT HULKA UTERINE TENACULUM FORCEPS
K944670 JARIT RECOMMENDED SINUS INSTRUMENTS
K944870 JARIT ENDOSCOPES, MODELS 600-600; 600-630; 600-650; AND 600-680
K941565 JARIT RECOMMENDED SINUS INSTRUMENTS
K932456 JARIT SURGICAL INSTRUMENTS
K933728 JARIT SURGICAL INSTRUMENTS: CATALOG 615-330, 615-331, 615-334, 615-335, 615-338, 615-339
K931928 JARIT SURGICAL INSTRUMENTS
K931959 JARIT SURGICAL INSTRUMENTS
K931878 JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680
K771625 LEININGEO AORTIC PUNCH #310-395 & 397
Search all 11 clearances from J. Jamner Surgical Instruments, Inc. →