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FDA 510(k)

MICROWAVAE DELIVERY SYSTEM #MW2000

K-Number: K010589 · 2001-03-19

Decision Date2001-03-19
Product CodeMWY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROWAVAE DELIVERY SYSTEM #MW2000 is the device name listed in this FDA 510(k) record. The listed applicant is Mw Medical, Inc.. It received FDA 510(k) clearance on 2001-03-19 under 510(k) number K010589. The device is classified under product code MWY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROWAVAE DELIVERY SYSTEM #MW2000?

MICROWAVAE DELIVERY SYSTEM #MW2000 is a medical device that received FDA 510(k) clearance on 2001-03-19. The listed applicant is Mw Medical, Inc.. The 510(k) number is K010589.

When did MICROWAVAE DELIVERY SYSTEM #MW2000 receive FDA 510(k) clearance?

MICROWAVAE DELIVERY SYSTEM #MW2000 received FDA 510(k) clearance on 2001-03-19, under 510(k) number K010589.

Who is the listed applicant for MICROWAVAE DELIVERY SYSTEM #MW2000?

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

What is the FDA product code for MICROWAVAE DELIVERY SYSTEM #MW2000?

The FDA product code for MICROWAVAE DELIVERY SYSTEM #MW2000 is MWY.

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.

Related Devices (Code: MWY)

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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