Q-HTF, CAT# 2001
K-Number: K993484 · 2000-05-25
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Device Summary
Frequently Asked Questions
What is the Q-HTF, CAT# 2001?
Q-HTF, CAT# 2001 is a medical device that received FDA 510(k) clearance on 2000-05-25. The listed applicant is Invitrocare, Inc.. The 510(k) number is K993484.
When did Q-HTF, CAT# 2001 receive FDA 510(k) clearance?
Q-HTF, CAT# 2001 received FDA 510(k) clearance on 2000-05-25, under 510(k) number K993484.
Who is the listed applicant for Q-HTF, CAT# 2001?
The FDA 510(k) record lists Invitrocare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Q-HTF, CAT# 2001?
The FDA product code for Q-HTF, CAT# 2001 is MQL.
Other records listing Invitrocare, 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: MQL)
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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