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FDA 510(k)

TIME WATCH

K-Number: K772119 · 1977-11-14

ApplicantAkzona, Inc.
Decision Date1977-11-14
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TIME WATCH is the device name listed in this FDA 510(k) record. The listed applicant is Akzona, Inc.. It received FDA 510(k) clearance on 1977-11-14 under 510(k) number K772119. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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