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FDA 510(k)

ULTRA SHIELD PF

K-Number: K934171 · 1994-02-01

ApplicantMedical Resources International, Inc.
Decision Date1994-02-01
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ULTRA SHIELD PF is the device name listed in this FDA 510(k) record. The listed applicant is Medical Resources International, Inc.. It received FDA 510(k) clearance on 1994-02-01 under 510(k) number K934171. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA SHIELD PF?

ULTRA SHIELD PF is a medical device that received FDA 510(k) clearance on 1994-02-01. The listed applicant is Medical Resources International, Inc.. The 510(k) number is K934171.

When did ULTRA SHIELD PF receive FDA 510(k) clearance?

ULTRA SHIELD PF received FDA 510(k) clearance on 1994-02-01, under 510(k) number K934171.

Who is the listed applicant for ULTRA SHIELD PF?

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

What is the FDA product code for ULTRA SHIELD PF?

The FDA product code for ULTRA SHIELD PF is LYY.

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.

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Other records listing Medical Resources International, 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.

K932702ULTAR-SHIELD

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Official Source

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