SELECTATEC SYSTEM
K-Number: K760668 · 1976-09-27
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Device Summary
Frequently Asked Questions
What is the SELECTATEC SYSTEM?
SELECTATEC SYSTEM is a medical device that received FDA 510(k) clearance on 1976-09-27. The listed applicant is Medishield, Inc.. The 510(k) number is K760668.
When did SELECTATEC SYSTEM receive FDA 510(k) clearance?
SELECTATEC SYSTEM received FDA 510(k) clearance on 1976-09-27, under 510(k) number K760668.
Who is the listed applicant for SELECTATEC SYSTEM?
The FDA 510(k) record lists Medishield, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SELECTATEC SYSTEM?
The FDA product code for SELECTATEC SYSTEM is CAD.
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 Medishield, 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: CAD)
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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