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FDA 510(k)

AUTOMATIC SHUT-OFF VALVE

K-Number: K760895 · 1976-12-09

Decision Date1976-12-09
Product CodeKZD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC SHUT-OFF VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Delta Medical Industries. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K760895. The device is classified under product code KZD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC SHUT-OFF VALVE?

AUTOMATIC SHUT-OFF VALVE is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Delta Medical Industries. The 510(k) number is K760895.

When did AUTOMATIC SHUT-OFF VALVE receive FDA 510(k) clearance?

AUTOMATIC SHUT-OFF VALVE received FDA 510(k) clearance on 1976-12-09, under 510(k) number K760895.

Who is the listed applicant for AUTOMATIC SHUT-OFF VALVE?

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

What is the FDA product code for AUTOMATIC SHUT-OFF VALVE?

The FDA product code for AUTOMATIC SHUT-OFF VALVE is KZD.

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 Delta Medical Industries 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.

View all 27 devices →

Related Devices (Code: KZD)

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

View on FDA Database →

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

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