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FDA 510(k)

S/D 600 SPHYGMOMANOMETER AND PULSEMETER

K-Number: K780805 · 1978-06-06

ApplicantG & W Applied Science Laboratories
Decision Date1978-06-06
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

S/D 600 SPHYGMOMANOMETER AND PULSEMETER is the device name listed in this FDA 510(k) record. The listed applicant is G & W Applied Science Laboratories. It received FDA 510(k) clearance on 1978-06-06 under 510(k) number K780805. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S/D 600 SPHYGMOMANOMETER AND PULSEMETER?

S/D 600 SPHYGMOMANOMETER AND PULSEMETER is a medical device that received FDA 510(k) clearance on 1978-06-06. The listed applicant is G & W Applied Science Laboratories. The 510(k) number is K780805.

When did S/D 600 SPHYGMOMANOMETER AND PULSEMETER receive FDA 510(k) clearance?

S/D 600 SPHYGMOMANOMETER AND PULSEMETER received FDA 510(k) clearance on 1978-06-06, under 510(k) number K780805.

Who is the listed applicant for S/D 600 SPHYGMOMANOMETER AND PULSEMETER?

The FDA 510(k) record lists G & W Applied Science Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for S/D 600 SPHYGMOMANOMETER AND PULSEMETER?

The FDA product code for S/D 600 SPHYGMOMANOMETER AND PULSEMETER is DXN.

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 G & W Applied Science Laboratories 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.

K813249HELP-MATEK7806774600 RECORDERK780566HEALTH SEAT SYSTEM

Related Devices (Code: DXN)

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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