FDA 510(k) Unknown 🇺🇸 United States

ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHR

K Number: K852018 · Decision Jul 11, 1985
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
20
Review Days
64

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
ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHR
K Number
K852018
Clearance Type
Traditional
Decision
Unknown
Applicant
Manan Manufacturing Co., Inc.
Date Received
May 8, 1985
Decision Date
July 11, 1985
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Other Clearances by Manan Manufacturing Co., Inc.

K Number Device Name
K873208 MANAN TURNER STYLE NEEDLE
K864405 MANAN CONTRAST MEDIA ADMINISTRATION SET
K863848 MANAN BREST TUMOR LOCALIZATION NEEDLE
K852501 MYELOGRAM PROCEDURE TRAY
K851832 NAMAN POTTS COURNAND NEEDLE
K851834 MANAN GWI GUIDE WIRE INTRODUCER
K851833 MANAN SELDINGER NEEDLE
K852426 MANAN TROCAR STYLE BIOPSY NEEDLE
K852427 MANAN SPINAL NEEDLE
K852428 MANAN EPIDURAL NEEDLE
Search all 20 clearances from Manan Manufacturing Co., Inc. →