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

INTRAVENOUS INJECTION SET

K Number: K841717 · Decision Jul 23, 1984
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
11
Review Days
89

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
INTRAVENOUS INJECTION SET
K Number
K841717
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Philadelphia Biologics Center
Date Received
April 25, 1984
Decision Date
July 23, 1984
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 Philadelphia Biologics Center

K Number Device Name
K834256 PBC SYRINGE IRRIGATING
K834255 PBC SCALP VEIN SET
K834254 PBC IV SET VENTED
K834252 PBC EXTENSION SET
K834253 PBC IV SET NON-VENTED
K820911 PBC NEEDLE BY NIPRO MED. INDUSTRIES
K813649 PBC NEEDLE
K813646 JMS DISPOSABLE SYRINGE
K813648 JMS NEEDLE & MAC JECT
K813647 PBC SYRINGE
Search all 11 clearances from Philadelphia Biologics Center →