NPH-KLENZ
K-Number: K940263 · 1994-05-18
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Device Summary
Frequently Asked Questions
What is the NPH-KLENZ?
NPH-KLENZ is a medical device that received FDA 510(k) clearance on 1994-05-18. The listed applicant is Calgon Corp.. The 510(k) number is K940263.
When did NPH-KLENZ receive FDA 510(k) clearance?
NPH-KLENZ received FDA 510(k) clearance on 1994-05-18, under 510(k) number K940263.
Who is the listed applicant for NPH-KLENZ?
The FDA 510(k) record lists Calgon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NPH-KLENZ?
The FDA product code for NPH-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 Corp. 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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