5 - IN - 1 CONNECTOR
K-Number: K864964 · 1987-01-20
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Device Summary
Frequently Asked Questions
What is the 5 - IN - 1 CONNECTOR?
5 - IN - 1 CONNECTOR is a medical device that received FDA 510(k) clearance on 1987-01-20. The listed applicant is Medovations, Inc.. The 510(k) number is K864964.
When did 5 - IN - 1 CONNECTOR receive FDA 510(k) clearance?
5 - IN - 1 CONNECTOR received FDA 510(k) clearance on 1987-01-20, under 510(k) number K864964.
Who is the listed applicant for 5 - IN - 1 CONNECTOR?
The FDA 510(k) record lists Medovations, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 5 - IN - 1 CONNECTOR?
The FDA product code for 5 - IN - 1 CONNECTOR is GAZ.
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 Medovations, 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: GAZ)
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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