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

PHARMA-PLAST CONNECTING TUBE TYPE SUCT-

K Number: K843470 · Decision Nov 16, 1984
Classifications
1
FEI Numbers
174
Registration Numbers
174
Same Product Code
23
Applicant Total
17
Review Days
71

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
PHARMA-PLAST CONNECTING TUBE TYPE SUCT-
K Number
K843470
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Zimmar Consulting , Ltd.
Date Received
September 6, 1984
Decision Date
November 16, 1984
Product Code
BYY
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
BYY Tube, Aspirating, Flexible, Connecting

Similar 510(k) Clearances

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

View all

Other Clearances by Zimmar Consulting , Ltd.

K Number Device Name
K860322 CLINISET INFUSION SET
K843477 PHARMA-PLAST RECTAL TIP
K843478 PHARMA-PLAST URIDROP-URIDOME
K843468 PHARMA-PLAST SUCTION SET TYPE YANKAUER
K843469 PHARMA-PLAST SUCTION TIP, TYPE ORTHOPAE-
K843466 PHARMA-PLAST OXYGEN CATHETER
K843467 PHARMA-PLAST NASAL OXYGEN CANNULA
K843475 PHARMA-PLAST SINGLE USE OVERSHOES
K843471 PHARMA-PLAST SYRINGE
K843473 PHARMA-PLAST INSULIN SYRINGE
Search all 17 clearances from Zimmar Consulting , Ltd. →