REFLEX(R) ESP
K-Number: K924881 · 1993-07-23
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Device Summary
Frequently Asked Questions
What is the REFLEX(R) ESP?
REFLEX(R) ESP is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Richard-Allan Medical. The 510(k) number is K924881.
When did REFLEX(R) ESP receive FDA 510(k) clearance?
REFLEX(R) ESP received FDA 510(k) clearance on 1993-07-23, under 510(k) number K924881.
Who is the listed applicant for REFLEX(R) ESP?
The FDA 510(k) record lists Richard-Allan Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REFLEX(R) ESP?
The FDA product code for REFLEX(R) ESP is GEI.
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 Richard-Allan Medical 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: GEI)
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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