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FDA 510(k)

MULTI-PURPOSE HOLDER

K-Number: K884630 · 1988-11-22

ApplicantMed-Dex Intl.
Decision Date1988-11-22
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTI-PURPOSE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Med-Dex Intl.. It received FDA 510(k) clearance on 1988-11-22 under 510(k) number K884630. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-PURPOSE HOLDER?

MULTI-PURPOSE HOLDER is a medical device that received FDA 510(k) clearance on 1988-11-22. The listed applicant is Med-Dex Intl.. The 510(k) number is K884630.

When did MULTI-PURPOSE HOLDER receive FDA 510(k) clearance?

MULTI-PURPOSE HOLDER received FDA 510(k) clearance on 1988-11-22, under 510(k) number K884630.

Who is the listed applicant for MULTI-PURPOSE HOLDER?

The FDA 510(k) record lists Med-Dex Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI-PURPOSE HOLDER?

The FDA product code for MULTI-PURPOSE HOLDER is LDQ.

Related Clinical Trials

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Other records listing Med-Dex Intl. 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.

K893569QUICK CHANGE MONTGOMERY STRAPK881083GENERAL PURPOSE KITK881084UTILITY CLAMP

Related Devices (Code: LDQ)

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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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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