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FDA 510(k)

RIGHT TIME RHYTHM CLOCK

K-Number: K823463 · 1983-03-17

ApplicantP.K. Morgan Instruments, Inc.
Decision Date1983-03-17
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

RIGHT TIME RHYTHM CLOCK is the device name listed in this FDA 510(k) record. The listed applicant is P.K. Morgan Instruments, Inc.. It received FDA 510(k) clearance on 1983-03-17 under 510(k) number K823463. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIGHT TIME RHYTHM CLOCK?

RIGHT TIME RHYTHM CLOCK is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is P.K. Morgan Instruments, Inc.. The 510(k) number is K823463.

When did RIGHT TIME RHYTHM CLOCK receive FDA 510(k) clearance?

RIGHT TIME RHYTHM CLOCK received FDA 510(k) clearance on 1983-03-17, under 510(k) number K823463.

Who is the listed applicant for RIGHT TIME RHYTHM CLOCK?

The FDA 510(k) record lists P.K. Morgan Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIGHT TIME RHYTHM CLOCK?

The FDA product code for RIGHT TIME RHYTHM CLOCK is LHD.

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.

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Other records listing P.K. Morgan Instruments, 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.

K830995POCKET SPIROMETER

Related Devices (Code: LHD)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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