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

OMNIMED I.V. SOLUTION ADMIN. SET

K Number: K853255 · Decision Aug 23, 1985
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
12
Review Days
21

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
OMNIMED I.V. SOLUTION ADMIN. SET
K Number
K853255
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Omni Intl., Inc.
Date Received
August 2, 1985
Decision Date
August 23, 1985
Product Code
FPA
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
FPA Set, Administration, Intravascular

Similar 510(k) Clearances

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

View all

Other Clearances by Omni Intl., Inc.

K Number Device Name
K984066 OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM
K984064 OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE
K851938 OMNIMED SURGICAL GOWN
K851654 OMNIMED CLAMP
K851734 OMNIMED SUPERIOR TRANSDUCER PROTECTOR
K850706 F-SERIES IMPLANT
K850112 OMNIMED IV SOLUTION ADMINISTRATION SET
K850066 OMNIMED NASAL OXYGEN CANNULA
K831147 OMNIPROBE ELECTRICAL NERVE STIMULATOR
K821523 OMNI TENS
Search all 12 clearances from Omni Intl., Inc. →