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FDA 510(k)

PRESERV SAF FIXATIVE 15ML

K-Number: K834566 · 1984-02-04

Decision Date1984-02-04
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PRESERV SAF FIXATIVE 15ML is the device name listed in this FDA 510(k) record. The listed applicant is Preventive Diagnostics Corp.. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K834566. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESERV SAF FIXATIVE 15ML?

PRESERV SAF FIXATIVE 15ML is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Preventive Diagnostics Corp.. The 510(k) number is K834566.

When did PRESERV SAF FIXATIVE 15ML receive FDA 510(k) clearance?

PRESERV SAF FIXATIVE 15ML received FDA 510(k) clearance on 1984-02-04, under 510(k) number K834566.

Who is the listed applicant for PRESERV SAF FIXATIVE 15ML?

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

What is the FDA product code for PRESERV SAF FIXATIVE 15ML?

The FDA product code for PRESERV SAF FIXATIVE 15ML is LIO.

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 Preventive Diagnostics Corp. 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 18 devices →

Related Devices (Code: LIO)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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