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

X-RAY MARKER

K Number: K882519 · Decision Aug 9, 1988
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
17
Applicant Total
17
Review Days
53

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Basic Information

Device Name
X-RAY MARKER
K Number
K882519
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1640
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Karlin Technology, Inc.
Date Received
June 17, 1988
Decision Date
August 9, 1988
Product Code
JAC
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
JAC System, X-Ray, Film Marking, Radiographic

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Other Clearances by Karlin Technology, Inc.

K Number Device Name
K903969 SUCTION RETRACTOR(TOWER ATTACH.)FOR CRANK FRAM RET
K893201 BONE PLATE
K893203 BONE SCREW
K882525 SPINAL MICROKNIFE
K882520 SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS
K882073 SPINAL NEEDLE
K882524 UNIVERSALLY ADJUSTABLE ARMBOARD
K882069 SPINAL DISTRACTORS, SPANNERS
K882072 ORTHOPAEDIC AND SPINAL RING CURRETTES
K882077 MICRODISCECTOMY CURRETTES
Search all 17 clearances from Karlin Technology, Inc. →