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

BONE MARROW BIOPSY TRAY

K Number: K912074 · Decision Aug 28, 1991
Classifications
1
FEI Numbers
321
Registration Numbers
322
Same Product Code
106
Applicant Total
39
Review Days
110

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Basic Information

Device Name
BONE MARROW BIOPSY TRAY
K Number
K912074
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Manan Medical Products, Inc.
Date Received
May 10, 1991
Decision Date
August 28, 1991
Product Code
GAA
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
GAA Needle, Aspiration And Injection, Disposable

Similar 510(k) Clearances

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Other Clearances by Manan Medical Products, Inc.

K Number Device Name
K052802 MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE
K011209 MANAN SPRITACRE SPINAL NEEDLES
K983620 MANAN SPINAL NEEDLES
K980536 EPIDURAL NEEDLE
K981386 MANAN BLUNT NEEDLE
K980211 MRI CHIBA,SPINAL,BREAST LOCALIZATION,AUTOMATIC CUTTING NEEDLES
K974446 MANAN AUTOMATIC CUTTING NEEDLE
K962977 MRI COMPATIBLE BIOPSY NEEDLES
K963767 MANAN V.S. ACCESS NEEDLE/SET
K961986 MANAN D BAG
Search all 39 clearances from Manan Medical Products, Inc. →