TIME WATCH
K-Number: K772119 · 1977-11-14
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Device Summary
Frequently Asked Questions
What is the TIME WATCH?
TIME WATCH is a medical device that received FDA 510(k) clearance on 1977-11-14. The listed applicant is Akzona, Inc.. The 510(k) number is K772119.
When did TIME WATCH receive FDA 510(k) clearance?
TIME WATCH received FDA 510(k) clearance on 1977-11-14, under 510(k) number K772119.
Who is the listed applicant for TIME WATCH?
The FDA 510(k) record lists Akzona, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TIME WATCH?
The FDA product code for TIME WATCH is FPK.
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 Akzona, 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: FPK)
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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