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FDA 510(k)

DELIVERY TUBE SET #2226

K-Number: K822761 · 1982-09-30

Decision Date1982-09-30
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DELIVERY TUBE SET #2226 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 1982-09-30 under 510(k) number K822761. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELIVERY TUBE SET #2226?

DELIVERY TUBE SET #2226 is a medical device that received FDA 510(k) clearance on 1982-09-30. The listed applicant is Delta Medical Industries. The 510(k) number is K822761.

When did DELIVERY TUBE SET #2226 receive FDA 510(k) clearance?

DELIVERY TUBE SET #2226 received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822761.

Who is the listed applicant for DELIVERY TUBE SET #2226?

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 DELIVERY TUBE SET #2226?

The FDA product code for DELIVERY TUBE SET #2226 is FRN.

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: FRN)

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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