FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

PIPER, MODEL NUMBER UDS-PIPERB

K Number: K951805 · Decision Jul 6, 1995
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
35
Applicant Total
11
Review Days
79

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Basic Information

Device Name
PIPER, MODEL NUMBER UDS-PIPERB
K Number
K951805
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1620
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Laborie Medical Technologies, Ltd.
Date Received
April 18, 1995
Decision Date
July 6, 1995
Product Code
FEN
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
FEN Device, Cystometric, Hydraulic

Similar 510(k) Clearances

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Other Clearances by Laborie Medical Technologies, Ltd.

K Number Device Name
K090830 LABORIE INJETAK ADJUSTABLE TIP NEEDLE, FLEXIBLE TIP AND RIDGID TIP
K962009 UROSTYM
K955856 TEX-AID BLUE
K955810 U-TEX
K942563 ELITE BIOFEEDBACK
K942023 INFUSION PUMP, MODEL NO. UDP-5
K934369 DRI SLEEPER
K931574 ADVANCE MODEL UDS-ADV
K930005 DRITRAINER
K924086 NICKI, MODEL NUMBER USD-NK-UP1
Search all 11 clearances from Laborie Medical Technologies, Ltd. →