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FDA 510(k)

DOUBLE TRACH SWIVEL CONNECTOR

K-Number: K935821 · 1994-01-14

ApplicantNutec, Inc.
Decision Date1994-01-14
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DOUBLE TRACH SWIVEL CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Nutec, Inc.. It received FDA 510(k) clearance on 1994-01-14 under 510(k) number K935821. 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 SWIVEL CONNECTOR?

DOUBLE TRACH SWIVEL CONNECTOR is a medical device that received FDA 510(k) clearance on 1994-01-14. The listed applicant is Nutec, Inc.. The 510(k) number is K935821.

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

DOUBLE TRACH SWIVEL CONNECTOR received FDA 510(k) clearance on 1994-01-14, under 510(k) number K935821.

Who is the listed applicant for DOUBLE TRACH SWIVEL CONNECTOR?

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

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

The FDA product code for DOUBLE TRACH SWIVEL 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.

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Other records listing Nutec, Inc. 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.

K940257HAND-HELD NEBULIZERK940255HYPERINFLATION BAG SYSTEM

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.

K083702TRACH-ASSISTMergenet MedicalK954383SURELOC CIRCUIT CONNECTORPolamedco, Inc.K954197DISPOSABLE FLEX TUBEEngstrom MedicalK953786UNICOR, INC. CONNECTORS & AIRWAY EXTENSIONSUnicor, Inc.K952824NEO-LINK, DISPOSABLE NEONATAL AIR WAY CONNECTORIntertex Medical, Inc.K951345DISPOSABLE AIRWAY CONNECTORS FOR GAS SAMPLINGCatheter Research, Inc.

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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