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

(ROTH)SPIRAL ROTATING PROSTATIC BIOPSY NEEDLE

K Number: K863385 · Decision Nov 4, 1986
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
63
Applicant Total
104
Review Days
62

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Basic Information

Device Name
(ROTH)SPIRAL ROTATING PROSTATIC BIOPSY NEEDLE
K Number
K863385
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3920
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Cook Urological, Inc.
Date Received
September 3, 1986
Decision Date
November 4, 1986
Product Code
KNN
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNN Components, Wheelchair

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