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

PALPATION PROBE

K Number: K911159 · Decision Mar 29, 1991
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
55
Review Days
14

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Basic Information

Device Name
PALPATION PROBE
K Number
K911159
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Northgate Technologies, Inc.
Date Received
March 15, 1991
Decision Date
March 29, 1991
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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K041560 FLO-ASSISTANT
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K022052 40LPM ABDOMINAL INSUFFLATOR, CATALOG # 72-00203-0
K010053 HUMI-FLOW, MODEL 6-850-00/ 01/02
K011928 HYDROTOWER ARTHROSCOPIC ADMINISTRATION TUBING SET, MODEL 7-460-05
K001325 FLO ASSISTANT, MODEL 4-250-00
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