FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MDT/CASTLE PURUS DENTAL UNIT

K Number: K914697 · Decision Nov 13, 1991
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
22
Review Days
26

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Basic Information

Device Name
MDT/CASTLE PURUS DENTAL UNIT
K Number
K914697
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mdt Corp., Inc.
Date Received
October 18, 1991
Decision Date
November 13, 1991
Product Code
EIA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EIA Unit, Operative Dental

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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
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. →