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

STEAROTHERMOHILUS SPORE STRIPS

K Number: K800482 · Decision Apr 16, 1980
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
205
Applicant Total
22
Review Days
43

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Basic Information

Device Name
STEAROTHERMOHILUS SPORE STRIPS
K Number
K800482
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Mdt Corp., Inc.
Date Received
March 4, 1980
Decision Date
April 16, 1980
Product Code
FRC
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
FRC Indicator, Biological Sterilization Process

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Other Clearances by Mdt Corp., Inc.

K Number Device Name
K960777 MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATOR
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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. →