FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

3-WAY STOPCOCK WITH LUER-LOCK FITTING

K Number: K770154 · Decision Feb 28, 1977
Classifications
1
FEI Numbers
214
Registration Numbers
214
Same Product Code
28
Applicant Total
10
Review Days
35

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Basic Information

Device Name
3-WAY STOPCOCK WITH LUER-LOCK FITTING
K Number
K770154
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
American Viggo
Date Received
January 24, 1977
Decision Date
February 28, 1977
Product Code
KGZ
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
KGZ Accessories, Catheter

Similar 510(k) Clearances

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

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Other Clearances by American Viggo

K Number Device Name
K771339 MALE LUER LOCK PLUG
K770528 NEEDLE, MEMBRANE
K770181 I.V. CATHETER PLACEMENT UNIT
K770174 LUER-LOCK EXTENSION SET
K770096 EPIDURAL BLOCK PROCEDURE PACK
K760666 4-WAY STOPCOCK W/LUER-LOCK FITTING
K760679 4-WAY STOPCOCK W/7CM TUBING,
K760678 4-WAY STOPCOCK W/100 CM TUBING, LUER-LK
K760667 4-WAY STOPCOCK W/10 CM EXTEN. TUBING