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

10CC SYRINGE CONTROL RING SET

K Number: K874747 · Decision Feb 4, 1988
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
16
Review Days
78

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Basic Information

Device Name
10CC SYRINGE CONTROL RING SET
K Number
K874747
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Procedure Products, Inc.
Date Received
November 18, 1987
Decision Date
February 4, 1988
Product Code
FMF
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
FMF Syringe, Piston

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Other Clearances by Procedure Products, Inc.

K Number Device Name
K161812 Freedom Syringe
K923194 INSUFFLATOR CONNECTING FILTER
K922536 TORQUE DEVICE
K914128 CONNECTING SET
K910673 BAG SPIGOT
K884985 MODIFIED 10CC SYRINGE CONTROL RING SET
K874037 ANGIO WASTE FLUIDS DUMP BAG
K853749 CUSTOM CORONARY MANIFOLD KITS
K842173 DISPOSABLE STOPCOCKS
K833554 MATERIAL ADDITION LEXAN & K-RESIN
Search all 16 clearances from Procedure Products, Inc. →