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

EFFNER FE-EX* OROGASTRIC

K Number: K874755 · Decision Apr 6, 1988
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
4
Review Days
140

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
EFFNER FE-EX* OROGASTRIC
K Number
K874755
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Effner and Spreine Co.
Date Received
November 18, 1987
Decision Date
April 6, 1988
Product Code
KNT
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
KNT Tubes, Gastrointestinal (And Accessories)

Similar 510(k) Clearances

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

View all

Other Clearances by Effner and Spreine Co.

K Number Device Name
K875260 EFFNER CAUTERY INSTRUMENTS
K872480 KAHN-TACT U.S.A., EFF LARYNGOSCOPE
K852014 EFFNER SIMS RECTAL SPECULUM W/FIBER OPTIC ILLUMINA