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FDA 510(k)

DOUBLE TRACH SEIVEL CONNECTOR

K-Number: K940544 · 1994-04-19

ApplicantFvtnks
Decision Date1994-04-19
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DOUBLE TRACH SEIVEL CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Fvtnks. It received FDA 510(k) clearance on 1994-04-19 under 510(k) number K940544. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOUBLE TRACH SEIVEL CONNECTOR?

DOUBLE TRACH SEIVEL CONNECTOR is a medical device that received FDA 510(k) clearance on 1994-04-19. The listed applicant is Fvtnks. The 510(k) number is K940544.

When did DOUBLE TRACH SEIVEL CONNECTOR receive FDA 510(k) clearance?

DOUBLE TRACH SEIVEL CONNECTOR received FDA 510(k) clearance on 1994-04-19, under 510(k) number K940544.

Who is the listed applicant for DOUBLE TRACH SEIVEL CONNECTOR?

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

What is the FDA product code for DOUBLE TRACH SEIVEL CONNECTOR?

The FDA product code for DOUBLE TRACH SEIVEL CONNECTOR is BZA.

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 Fvtnks 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.

Related Devices (Code: BZA)

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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