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

MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE

K Number: K924380 · Decision Feb 16, 1994
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
46
Applicant Total
22
Review Days
534

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE
K Number
K924380
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mdt Corp., Inc.
Date Received
August 31, 1992
Decision Date
February 16, 1994
Product Code
MLR
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
MLR Sterilizer, Chemical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MLR), ordered by most recent decision date.

View all

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
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. →