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

SIMPLASTIC SUPRA PUBIC CATHETER

K Number: K852200 · Decision Aug 7, 1985
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
31
Applicant Total
4
Review Days
78

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Basic Information

Device Name
SIMPLASTIC SUPRA PUBIC CATHETER
K Number
K852200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5090
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Franklin Medical USA, Inc.
Date Received
May 21, 1985
Decision Date
August 7, 1985
Product Code
KOB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KOB Catheter, Suprapubic (And Accessories)

Similar 510(k) Clearances

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

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Other Clearances by Franklin Medical USA, Inc.

K Number Device Name
K931488 KSF SPINAL FIXATOR
K884589 FRANTZ MEDICAL SHARPS COLLECTOR
K862478 HAYES VAGINAL SHIELD