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

SECURACATH CATHETER, MODEL SPK01

K Number: K082047 · Decision Sep 30, 2008
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
4
Applicant Total
7
Review Days
74

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Basic Information

Device Name
SECURACATH CATHETER, MODEL SPK01
K Number
K082047
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Interrad Medical, Inc.
Date Received
July 18, 2008
Decision Date
September 30, 2008
Product Code
OKC
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
OKC Implanted Subcutaneous Securement Catheter

Similar 510(k) Clearances

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

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Other Clearances by Interrad Medical, Inc.

K Number Device Name
K210629 SecurAcath
K180994 SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F
K180769 SecurAcath
K120935 SECURACATH
K092306 SECURACATH UNIVERSAL
K083081 MODIFICATION TO SECURACATH, MODEL: SPK01