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

MANAN D BAG

K Number: K963849 · Decision Dec 13, 1996
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
8
Applicant Total
39
Review Days
79

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Basic Information

Device Name
MANAN D BAG
K Number
K963849
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Manan Medical Products, Inc.
Date Received
September 25, 1996
Decision Date
December 13, 1996
Product Code
EXF
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
EXF Bag, Bile Collecting

Similar 510(k) Clearances

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

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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. →