ADCOMP
K-Number: K860610 · 1986-07-08
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Device Summary
Frequently Asked Questions
What is the ADCOMP?
ADCOMP is a medical device that received FDA 510(k) clearance on 1986-07-08. The listed applicant is Healthtek, Inc.. The 510(k) number is K860610.
When did ADCOMP receive FDA 510(k) clearance?
ADCOMP received FDA 510(k) clearance on 1986-07-08, under 510(k) number K860610.
Who is the listed applicant for ADCOMP?
The FDA 510(k) record lists Healthtek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADCOMP?
The FDA product code for ADCOMP is LHI.
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 Healthtek, 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: LHI)
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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