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

MDT UROLOGY TABLE

K Number: K942485 · Decision Aug 26, 1994
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
3
Applicant Total
22
Review Days
93

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Basic Information

Device Name
MDT UROLOGY TABLE
K Number
K942485
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4890
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mdt Corp., Inc.
Date Received
May 25, 1994
Decision Date
August 26, 1994
Product Code
MMZ
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
MMZ Table, Cystometric, Electric

Similar 510(k) Clearances

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Other Clearances by Mdt Corp., Inc.

K Number Device Name
K960777 MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATOR
K942486 IMAGE FULL POWER EXAMINATION/MINOR SURGERY TABLE
K924380 MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE
K926081 DENTAL LIGHT
K924955 MDT/HARVEY MC-8 AND MC-10
K932094 BOVIE ULTRASONIC SURGICAL ASPIRATOR
K931169 MDT DENTAL CHAIR
K920930 MDT/CASTLE 10/90 DUAL LOAD STATION
K922212 MDT CASTLE BIOSIGN TEST PACK
K914758 MDT/SHAMPAINE MODEL 4900B SURGICAL TABLE
Search all 22 clearances from Mdt Corp., Inc. →