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FDA 510(k)

PULSAR PULSE MONITOR WATCH

K-Number: K760710 · 1976-12-02

ApplicantTime Computer, Inc. (Tci)
Decision Date1976-12-02
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PULSAR PULSE MONITOR WATCH is the device name listed in this FDA 510(k) record. The listed applicant is Time Computer, Inc. (Tci). It received FDA 510(k) clearance on 1976-12-02 under 510(k) number K760710. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULSAR PULSE MONITOR WATCH?

PULSAR PULSE MONITOR WATCH is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is Time Computer, Inc. (Tci). The 510(k) number is K760710.

When did PULSAR PULSE MONITOR WATCH receive FDA 510(k) clearance?

PULSAR PULSE MONITOR WATCH received FDA 510(k) clearance on 1976-12-02, under 510(k) number K760710.

Who is the listed applicant for PULSAR PULSE MONITOR WATCH?

The FDA 510(k) record lists Time Computer, Inc. (Tci) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PULSAR PULSE MONITOR WATCH?

The FDA product code for PULSAR PULSE MONITOR WATCH is DRT.

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Related Devices (Code: DRT)

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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