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

DISCOGRAPHY KIT

K Number: K960082 · Decision Mar 21, 1996
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
6
Applicant Total
8
Review Days
70

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Basic Information

Device Name
DISCOGRAPHY KIT
K Number
K960082
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1730
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Spinal Specialties, Inc.
Date Received
January 11, 1996
Decision Date
March 21, 1996
Product Code
IZG
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IZG System, X-Ray, Photofluorographic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IZG), ordered by most recent decision date.

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Other Clearances by Spinal Specialties, Inc.

K Number Device Name
K960100 SPINAL SPECIALTIES NERVE BLOCK TRAY
K942863 EPIDURAL NEEDLE
K950820 SPINAL SPECIALTIES PENCIL-POINT SPINAL NEEDLE
K943319 GERTIE MARX EPI-SPINAL TRAY
K944029 CONTINUOUS EPIDURAL ANESTHESIA TRAY
K941343 SPINAL ANESTHESIA TRAY
K935245 EPIDURAL ANESTHESIA TRAY