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

REBUILDING STERILIZERS

K Number: K882713 · Decision Aug 12, 1988
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
183
Applicant Total
22
Review Days
42

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Basic Information

Device Name
REBUILDING STERILIZERS
K Number
K882713
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6880
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Mdt Corp., Inc.
Date Received
July 1, 1988
Decision Date
August 12, 1988
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
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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
Search all 22 clearances from Mdt Corp., Inc. →