QUEST DIAGNOSTICS HAIRCHECK-DT (PCP
K-Number: K042726 · 2005-07-28
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Device Summary
Frequently Asked Questions
What is the QUEST DIAGNOSTICS HAIRCHECK-DT (PCP?
QUEST DIAGNOSTICS HAIRCHECK-DT (PCP is a medical device that received FDA 510(k) clearance on 2005-07-28. The listed applicant is Quest Diagnostics, Inc.. The 510(k) number is K042726.
When did QUEST DIAGNOSTICS HAIRCHECK-DT (PCP receive FDA 510(k) clearance?
QUEST DIAGNOSTICS HAIRCHECK-DT (PCP received FDA 510(k) clearance on 2005-07-28, under 510(k) number K042726.
Who is the listed applicant for QUEST DIAGNOSTICS HAIRCHECK-DT (PCP?
The FDA 510(k) record lists Quest Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUEST DIAGNOSTICS HAIRCHECK-DT (PCP?
The FDA product code for QUEST DIAGNOSTICS HAIRCHECK-DT (PCP is LCM.
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 Quest Diagnostics, 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: LCM)
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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