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FDA 510(k)

MUFFLER GAS-AIR VENT UNIT

K-Number: K832170 · 1985-04-02

Decision Date1985-04-02
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MUFFLER GAS-AIR VENT UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Edward Richards. It received FDA 510(k) clearance on 1985-04-02 under 510(k) number K832170. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUFFLER GAS-AIR VENT UNIT?

MUFFLER GAS-AIR VENT UNIT is a medical device that received FDA 510(k) clearance on 1985-04-02. The listed applicant is Dr. Edward Richards. The 510(k) number is K832170.

When did MUFFLER GAS-AIR VENT UNIT receive FDA 510(k) clearance?

MUFFLER GAS-AIR VENT UNIT received FDA 510(k) clearance on 1985-04-02, under 510(k) number K832170.

Who is the listed applicant for MUFFLER GAS-AIR VENT UNIT?

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

What is the FDA product code for MUFFLER GAS-AIR VENT UNIT?

The FDA product code for MUFFLER GAS-AIR VENT UNIT is KNT.

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.

Related Devices (Code: KNT)

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.

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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