FDA 510(k)

HVG-100

K-Number: K790033 · 1979-02-09

Decision Date1979-02-09

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

HVG-100 is the device name listed in this FDA 510(k) record. The listed applicant is Elmed, Inc.. It received FDA 510(k) clearance on 1979-02-09 under 510(k) number K790033. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HVG-100?

HVG-100 is a medical device that received FDA 510(k) clearance on 1979-02-09. The listed applicant is Elmed, Inc.. The 510(k) number is K790033.

When did HVG-100 receive FDA 510(k) clearance?

HVG-100 received FDA 510(k) clearance on 1979-02-09, under 510(k) number K790033.

Who is the listed applicant for HVG-100?

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

What is the FDA product code for HVG-100?

The FDA product code for HVG-100 is IPF.

Other records listing Elmed, Inc. 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.

K010465DENSTAT K974793ELMED ESU 120 M/M DIGITAL K953271ELMED RF-ALERT K952110ELMED THERMO-FLUX K926517ELMED LBC 50-P K932938ELMED ESU 300 M/M AND DIGITAL

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Related Devices (Code: IPF)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.