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

MANAN MENGHINI NEEDLE

K Number: K851836 · Decision Jun 21, 1985
Classifications
1
FEI Numbers
207
Registration Numbers
207
Same Product Code
360
Applicant Total
20
Review Days
54

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
MANAN MENGHINI NEEDLE
K Number
K851836
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Manan Manufacturing Co., Inc.
Date Received
April 28, 1985
Decision Date
June 21, 1985
Product Code
KNW
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
KNW Instrument, Biopsy

Similar 510(k) Clearances

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

View all

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
K852018 ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHR
K852426 MANAN TROCAR STYLE BIOPSY NEEDLE
K852427 MANAN SPINAL NEEDLE
Search all 20 clearances from Manan Manufacturing Co., Inc. →