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FDA 510(k)

VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM

K-Number: K894695 · 1990-01-22

Decision Date1990-01-22
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medistad Corp.. It received FDA 510(k) clearance on 1990-01-22 under 510(k) number K894695. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM?

VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is Medistad Corp.. The 510(k) number is K894695.

When did VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM receive FDA 510(k) clearance?

VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM received FDA 510(k) clearance on 1990-01-22, under 510(k) number K894695.

Who is the listed applicant for VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM?

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

What is the FDA product code for VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM?

The FDA product code for VACUSAFE DISP. VACUUM - EXTRACTION SYSTEM is GCX.

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: GCX)

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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