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

EXCELSIOR SINGLE LEAD DISPENSING SET

K Number: K913804 · Decision Feb 11, 1992
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
5
Review Days
169

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
EXCELSIOR SINGLE LEAD DISPENSING SET
K Number
K913804
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Excel Medical, Inc.
Date Received
August 26, 1991
Decision Date
February 11, 1992
Product Code
LHI
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LHI Set, I.V. Fluid Transfer

Similar 510(k) Clearances

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

View all

Other Clearances by Excel Medical, Inc.

K Number Device Name
K932462 VENTED NEEDLE
K923966 SYRINGE ADAPTOR
K914988 500 INFUSER
K905116 PHARM-ASSIST