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

BIOLOGIC DT-1000 MACHINE

K Number: K923046 · Decision Sep 30, 1994
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
5
Review Days
828

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Basic Information

Device Name
BIOLOGIC DT-1000 MACHINE
K Number
K923046
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hemocleanse, Inc.
Date Received
June 24, 1992
Decision Date
September 30, 1994
Product Code
KNT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNT Tubes, Gastrointestinal (And Accessories)

Similar 510(k) Clearances

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

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Other Clearances by Hemocleanse, Inc.

K Number Device Name
K993330 THERMOCHEM-HT SYSTEM
K992196 BIOLOGIC-DT SYSTEM (BIOLOGIC-DT-1000 WITH DT-1000-TK)
K984546 BIOLOGIC-DT MACHINE, MODEL DT-1000 AND BIOLOGIC-DT TREATMENT KIT, MODEL DT-1000-TK
K953751 BIOLOGIC-DT SYSTEM