PIPET CURET
K-Number: K001545 · 2000-06-15
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Device Summary
Frequently Asked Questions
What is the PIPET CURET?
PIPET CURET is a medical device that received FDA 510(k) clearance on 2000-06-15. The listed applicant is Milex Products, Inc.. The 510(k) number is K001545.
When did PIPET CURET receive FDA 510(k) clearance?
PIPET CURET received FDA 510(k) clearance on 2000-06-15, under 510(k) number K001545.
Who is the listed applicant for PIPET CURET?
The FDA 510(k) record lists Milex Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PIPET CURET?
The FDA product code for PIPET CURET is HHK.
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 Milex Products, Inc. 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: HHK)
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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