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

ALSA-KLENZ

K Number: K944494 · Decision Oct 19, 1994
Classifications
1
FEI Numbers
150
Registration Numbers
150
Same Product Code
18
Applicant Total
19
Review Days
36

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Basic Information

Device Name
ALSA-KLENZ
K Number
K944494
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6150
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Calgon Vestal Div.
Date Received
September 13, 1994
Decision Date
October 19, 1994
Product Code
FLG
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
FLG Cleaner, Ultrasonic, Medical Instrument

Similar 510(k) Clearances

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

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Other Clearances by Calgon Vestal Div.

K Number Device Name
K944033 BILL EVANS-KLENZ
K942270 SAF-GEL HYDRATING DERMAL WOUND DRESSING
K931477 AMERSE
K931816 VESTA-SYDE(R) INTERIM INSTR DECONTAMINATION SYSTEM
K931342 LPH
K941163 MON-KLENZ
K931573 VESPHENE II
K932277 LONZA FORMULATION R-82
K931599 HYDRASORB STERILE DRESSING
K926034 EPI-LOCK WOUND DRESSING
Search all 19 clearances from Calgon Vestal Div. →