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FDA 510(k)

WESTMED RESPIRATORY LUER ADAPTOR

K-Number: K953506 · 1995-09-15

ApplicantWestmed Intl.
Decision Date1995-09-15
Product CodeBXY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

WESTMED RESPIRATORY LUER ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Westmed Intl.. It received FDA 510(k) clearance on 1995-09-15 under 510(k) number K953506. The device is classified under product code BXY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WESTMED RESPIRATORY LUER ADAPTOR?

WESTMED RESPIRATORY LUER ADAPTOR is a medical device that received FDA 510(k) clearance on 1995-09-15. The listed applicant is Westmed Intl.. The 510(k) number is K953506.

When did WESTMED RESPIRATORY LUER ADAPTOR receive FDA 510(k) clearance?

WESTMED RESPIRATORY LUER ADAPTOR received FDA 510(k) clearance on 1995-09-15, under 510(k) number K953506.

Who is the listed applicant for WESTMED RESPIRATORY LUER ADAPTOR?

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

What is the FDA product code for WESTMED RESPIRATORY LUER ADAPTOR?

The FDA product code for WESTMED RESPIRATORY LUER ADAPTOR is BXY.

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 Westmed Intl. 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 9 devices →

Related Devices (Code: BXY)

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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