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

TUBE, FEEDING, ARGYLE

K Number: K760137 · Decision Jul 16, 1976
Classifications
1
FEI Numbers
46
Registration Numbers
47
Same Product Code
58
Applicant Total
62
Review Days
18

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
TUBE, FEEDING, ARGYLE
K Number
K760137
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Sherwood Medical Industries
Date Received
June 28, 1976
Decision Date
July 16, 1976
Product Code
FPD
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
FPD Tube, Feeding

Similar 510(k) Clearances

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

View all

Other Clearances by Sherwood Medical Industries

K Number Device Name
K801070 SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES
K801071 LANCER GLUCOSE RATE REAGENT KIT
K792013 LANCER L-INA HUMAN REFERENCE SERUM
K792014 LANCER L-INA BUFFER, POLYMER, WASH SOLU
K782077 LANCER ICE CUBE
K790523 ARGYLE ESOPHAGEAL STETHOSCOPE
K790196 MONOJECT ARTERIAL BLOOD SAMPLING DEVICE
K790197 REAGENT KIT, LANCER GLUCOSE
K781459 MONOJECT SCALE MAGNIFIER
K781060 MONOJECT ENDOSSEOUS DENTAL IMPLANT
Search all 62 clearances from Sherwood Medical Industries →