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FDA 510(k)

WESTCO MADAYAG PAB NEEDLE

K-Number: K894387 · 1989-11-07

Decision Date1989-11-07
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

WESTCO MADAYAG PAB NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Western Medical, Ltd.. It received FDA 510(k) clearance on 1989-11-07 under 510(k) number K894387. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WESTCO MADAYAG PAB NEEDLE?

WESTCO MADAYAG PAB NEEDLE is a medical device that received FDA 510(k) clearance on 1989-11-07. The listed applicant is Western Medical, Ltd.. The 510(k) number is K894387.

When did WESTCO MADAYAG PAB NEEDLE receive FDA 510(k) clearance?

WESTCO MADAYAG PAB NEEDLE received FDA 510(k) clearance on 1989-11-07, under 510(k) number K894387.

Who is the listed applicant for WESTCO MADAYAG PAB NEEDLE?

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

What is the FDA product code for WESTCO MADAYAG PAB NEEDLE?

The FDA product code for WESTCO MADAYAG PAB NEEDLE is HAW.

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 Western Medical, Ltd. 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: HAW)

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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