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FDA 510(k)

GRAVIDAPHONE

K-Number: K802024 · 1981-01-07

ApplicantSolar Electronics
Decision Date1981-01-07
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GRAVIDAPHONE is the device name listed in this FDA 510(k) record. The listed applicant is Solar Electronics. It received FDA 510(k) clearance on 1981-01-07 under 510(k) number K802024. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAVIDAPHONE?

GRAVIDAPHONE is a medical device that received FDA 510(k) clearance on 1981-01-07. The listed applicant is Solar Electronics. The 510(k) number is K802024.

When did GRAVIDAPHONE receive FDA 510(k) clearance?

GRAVIDAPHONE received FDA 510(k) clearance on 1981-01-07, under 510(k) number K802024.

Who is the listed applicant for GRAVIDAPHONE?

The FDA 510(k) record lists Solar Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRAVIDAPHONE?

The FDA product code for GRAVIDAPHONE is KNG.

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Related Devices (Code: KNG)

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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