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

EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE)

K Number: K926218 · Decision Aug 26, 1994
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
64
Applicant Total
16
Review Days
624

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Basic Information

Device Name
EISMAN-TRIES MEP (MULTIPLE ELECTRODE PROBE)
K Number
K926218
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1425
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sandhill Scientific, Inc.
Date Received
December 10, 1992
Decision Date
August 26, 1994
Product Code
HIR
Advisory Committee
Obstetrics/Gynecology
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
HIR Perineometer

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K990441 INSIGHT SPHINCTER OF ODDI MANOMETRY MODULE, MODEL S981300
K984444 INSIGHT GASTROINTESTINAL MOTILITY SYSTEM, MODEL S980000
K961056 BIOVIEW MODEL S960000
K942247 SMALL BOWEL ANALYSIS SOFTWARE
K941801 ANALGRAPH
K931963 SANDHILL DISPOSABLE INTERNAL REFERENCE PH PROBE
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