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FDA 510(k)

GRAPHITE ATOMIZER, HGA-76B

K-Number: K770640 · 1977-06-24

Decision Date1977-06-24
Product Code
DecisionSubstantially Equivalent

Device Summary

GRAPHITE ATOMIZER, HGA-76B is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1977-06-24 under 510(k) number K770640. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAPHITE ATOMIZER, HGA-76B?

GRAPHITE ATOMIZER, HGA-76B is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K770640.

When did GRAPHITE ATOMIZER, HGA-76B receive FDA 510(k) clearance?

GRAPHITE ATOMIZER, HGA-76B received FDA 510(k) clearance on 1977-06-24, under 510(k) number K770640.

Who is the listed applicant for GRAPHITE ATOMIZER, HGA-76B?

The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

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 The Perkin-Elmer Corp. 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.

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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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