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FDA 510(k)

NON-REBREATHING T PIECE

K-Number: K790820 · 1979-05-04

Decision Date1979-05-04
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NON-REBREATHING T PIECE is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. It received FDA 510(k) clearance on 1979-05-04 under 510(k) number K790820. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-REBREATHING T PIECE?

NON-REBREATHING T PIECE is a medical device that received FDA 510(k) clearance on 1979-05-04. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K790820.

When did NON-REBREATHING T PIECE receive FDA 510(k) clearance?

NON-REBREATHING T PIECE received FDA 510(k) clearance on 1979-05-04, under 510(k) number K790820.

Who is the listed applicant for NON-REBREATHING T PIECE?

The FDA 510(k) record lists Dhd Medical Products Div. Diemolding Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NON-REBREATHING T PIECE?

The FDA product code for NON-REBREATHING T PIECE is CBP.

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 Dhd Medical Products Div. Diemolding Corp. 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 43 devices →

Related Devices (Code: CBP)

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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