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

MDT/HARVEY MC-8 AND MC-10

K Number: K924955 · Decision Oct 15, 1993
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
183
Applicant Total
22
Review Days
380

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Basic Information

Device Name
MDT/HARVEY MC-8 AND MC-10
K Number
K924955
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6880
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mdt Corp., Inc.
Date Received
September 30, 1992
Decision Date
October 15, 1993
Product Code
FLE
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
FLE Sterilizer, Steam

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Other Clearances by Mdt Corp., Inc.

K Number Device Name
K960777 MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATOR
K942485 MDT UROLOGY TABLE
K942486 IMAGE FULL POWER EXAMINATION/MINOR SURGERY TABLE
K924380 MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE
K926081 DENTAL LIGHT
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. →