ACCU GUIDE
K-Number: K984382 · 1999-03-05
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Device Summary
Frequently Asked Questions
What is the ACCU GUIDE?
ACCU GUIDE is a medical device that received FDA 510(k) clearance on 1999-03-05. The listed applicant is Tayman Medical, Inc.. The 510(k) number is K984382.
When did ACCU GUIDE receive FDA 510(k) clearance?
ACCU GUIDE received FDA 510(k) clearance on 1999-03-05, under 510(k) number K984382.
Who is the listed applicant for ACCU GUIDE?
The FDA 510(k) record lists Tayman Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACCU GUIDE?
The FDA product code for ACCU GUIDE is IYO.
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 Tayman Medical, 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: IYO)
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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