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FDA 510(k)

WESTMED CONDESATE COLLECTION TRAP

K-Number: K954271 · 1995-12-28

ApplicantWestmed Intl.
Decision Date1995-12-28
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

WESTMED CONDESATE COLLECTION TRAP is the device name listed in this FDA 510(k) record. The listed applicant is Westmed Intl.. It received FDA 510(k) clearance on 1995-12-28 under 510(k) number K954271. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WESTMED CONDESATE COLLECTION TRAP?

WESTMED CONDESATE COLLECTION TRAP is a medical device that received FDA 510(k) clearance on 1995-12-28. The listed applicant is Westmed Intl.. The 510(k) number is K954271.

When did WESTMED CONDESATE COLLECTION TRAP receive FDA 510(k) clearance?

WESTMED CONDESATE COLLECTION TRAP received FDA 510(k) clearance on 1995-12-28, under 510(k) number K954271.

Who is the listed applicant for WESTMED CONDESATE COLLECTION TRAP?

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 CONDESATE COLLECTION TRAP?

The FDA product code for WESTMED CONDESATE COLLECTION TRAP is CAW.

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: CAW)

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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