DERRICK SURESHIELD
K-Number: K953712 · 1995-10-12
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Device Summary
Frequently Asked Questions
What is the DERRICK SURESHIELD?
DERRICK SURESHIELD is a medical device that received FDA 510(k) clearance on 1995-10-12. The listed applicant is M.P.S. Pharm'L Int'L. The 510(k) number is K953712.
When did DERRICK SURESHIELD receive FDA 510(k) clearance?
DERRICK SURESHIELD received FDA 510(k) clearance on 1995-10-12, under 510(k) number K953712.
Who is the listed applicant for DERRICK SURESHIELD?
The FDA 510(k) record lists M.P.S. Pharm'L Int'L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DERRICK SURESHIELD?
The FDA product code for DERRICK SURESHIELD is KGO.
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 M.P.S. Pharm'L Int'L 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: KGO)
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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