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FDA 510(k)

MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT

K-Number: K944522 · 1995-02-24

Decision Date1995-02-24
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 1995-02-24 under 510(k) number K944522. The device is classified under product code IWJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT?

MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT is a medical device that received FDA 510(k) clearance on 1995-02-24. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K944522.

When did MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT receive FDA 510(k) clearance?

MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT received FDA 510(k) clearance on 1995-02-24, under 510(k) number K944522.

Who is the listed applicant for MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT?

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

What is the FDA product code for MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT?

The FDA product code for MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT is IWJ.

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 Medical Device Technologies, 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.

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Related Devices (Code: IWJ)

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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