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

SPINAL NEEDLE

K Number: K882073 · Decision Jul 18, 1988
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
47
Applicant Total
17
Review Days
62

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SPINAL NEEDLE
K Number
K882073
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Karlin Technology, Inc.
Date Received
May 17, 1988
Decision Date
July 18, 1988
Product Code
GDM
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
GDM Needle, Aspiration And Injection, Reusable

Similar 510(k) Clearances

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

View all

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
K882519 X-RAY MARKER
K882520 SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS
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. →