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

I.V. ADMINISTRATION SET

K Number: K810757 · Decision Apr 8, 1981
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
19
Applicant Total
13
Review Days
19

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
I.V. ADMINISTRATION SET
K Number
K810757
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
American Mcgaw
Date Received
March 20, 1981
Decision Date
April 8, 1981
Product Code
FDA
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
FDA Enteroscope And Accessories

Similar 510(k) Clearances

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

View all

Other Clearances by American Mcgaw

K Number Device Name
K853549 MCGAW/DROP WATCH FLOW MONITOR
K843639 ADD-A-VIAL SOLUTION TRANSFER DEVICE
K843954 MIXING CONTAINER
K841729 ACCUPRO ENTERAL FEEDING PUMP
K840212 CONCENTRATED PLATELET ADMIN. SET
K840388 PAB IV CONTAINER
K831716 CAPD - CATHETER ADAPTER
K822240 ETHYLENE OXIDE STERILIZ. PARAMETRIC REL.
K820133 MCGAW FAT EMULSION SET
K813092 ACCUPRO I.V. ADMINISTRATION SET
Search all 13 clearances from American Mcgaw →