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

THE GRIPPER SEAL(TM)

K Number: K870900 · Decision Mar 31, 1987
Classifications
1
FEI Numbers
972
Registration Numbers
972
Same Product Code
186
Applicant Total
43
Review Days
26

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Basic Information

Device Name
THE GRIPPER SEAL(TM)
K Number
K870900
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5240
Medical Specialty
General Hospital
Decision
Substantially Equivalent for Some Indications
Applicant
Pharmacia Deltec, Inc.
Date Received
March 5, 1987
Decision Date
March 31, 1987
Product Code
KGX
Advisory Committee
General Hospital
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
KGX Tape And Bandage, Adhesive

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Other Clearances by Pharmacia Deltec, Inc.

K Number Device Name
K943310 MODEL 6100 AMBULATORY INFUSION SYSTEM
K942046 PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE
K942161 LOCKBOX
K942024 PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEM
K941445 EXTENSION SET WITH ANTI-SIPHON VALVE
K931073 CATH-FINDER
K932430 DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER
K932433 PHERIPHERALLY INSERTED VENOUS CATHETER-Y SITE
K932198 PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH
K932464 PERIPHERALLYINSRTED VENOUS CATH. ALTERNATE CATH.
Search all 43 clearances from Pharmacia Deltec, Inc. →