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FDA 510(k)

DELTA D-750 THERMAFLOW

K-Number: K790406 · 1979-11-13

ApplicantDelta Medical Industries
Decision Date1979-11-13
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DELTA D-750 THERMAFLOW 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 1979-11-13 under 510(k) number K790406. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTA D-750 THERMAFLOW?

DELTA D-750 THERMAFLOW is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Delta Medical Industries. The 510(k) number is K790406.

When did DELTA D-750 THERMAFLOW receive FDA 510(k) clearance?

DELTA D-750 THERMAFLOW received FDA 510(k) clearance on 1979-11-13, under 510(k) number K790406.

Who is the listed applicant for DELTA D-750 THERMAFLOW?

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 DELTA D-750 THERMAFLOW?

The FDA product code for DELTA D-750 THERMAFLOW is DTZ.

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Other records listing Delta Medical Industries as applicant

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Related Devices (Code: DTZ)

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

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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