ALSA-KLENZ
K-Number: K944494 · 1994-10-19
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Device Summary
Frequently Asked Questions
What is the ALSA-KLENZ?
ALSA-KLENZ is a medical device that received FDA 510(k) clearance on 1994-10-19. The listed applicant is Calgon Vestal Div.. The 510(k) number is K944494.
When did ALSA-KLENZ receive FDA 510(k) clearance?
ALSA-KLENZ received FDA 510(k) clearance on 1994-10-19, under 510(k) number K944494.
Who is the listed applicant for ALSA-KLENZ?
The FDA 510(k) record lists Calgon Vestal Div. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALSA-KLENZ?
The FDA product code for ALSA-KLENZ is FLG.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Calgon Vestal Div. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FLG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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