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FDA 510(k)

GENERATOR, MODEL VG-1

K-Number: K790217 · 1979-02-06

ApplicantStreet Electronics Corp.
Decision Date1979-02-06
Product CodeGWE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

GENERATOR, MODEL VG-1 is the device name listed in this FDA 510(k) record. The listed applicant is Street Electronics Corp.. It received FDA 510(k) clearance on 1979-02-06 under 510(k) number K790217. The device is classified under product code GWE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERATOR, MODEL VG-1?

GENERATOR, MODEL VG-1 is a medical device that received FDA 510(k) clearance on 1979-02-06. The listed applicant is Street Electronics Corp.. The 510(k) number is K790217.

When did GENERATOR, MODEL VG-1 receive FDA 510(k) clearance?

GENERATOR, MODEL VG-1 received FDA 510(k) clearance on 1979-02-06, under 510(k) number K790217.

Who is the listed applicant for GENERATOR, MODEL VG-1?

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

What is the FDA product code for GENERATOR, MODEL VG-1?

The FDA product code for GENERATOR, MODEL VG-1 is GWE.

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Other records listing Street Electronics 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.

K781292CARDIOPNEUMOGRAPH

Related Devices (Code: GWE)

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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