ULTAR-SHIELD
K-Number: K932702 · 1994-03-07
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Device Summary
Frequently Asked Questions
What is the ULTAR-SHIELD?
ULTAR-SHIELD is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Medical Resources International, Inc.. The 510(k) number is K932702.
When did ULTAR-SHIELD receive FDA 510(k) clearance?
ULTAR-SHIELD received FDA 510(k) clearance on 1994-03-07, under 510(k) number K932702.
Who is the listed applicant for ULTAR-SHIELD?
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 ULTAR-SHIELD?
The FDA product code for ULTAR-SHIELD 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.
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.
Related Devices (Code: LYY)
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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