EVACU SLED
K-Number: K913520 · 1991-12-04
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Device Summary
Frequently Asked Questions
What is the EVACU SLED?
EVACU SLED is a medical device that received FDA 510(k) clearance on 1991-12-04. The listed applicant is Nexus Health Care Products , Ltd.. The 510(k) number is K913520.
When did EVACU SLED receive FDA 510(k) clearance?
EVACU SLED received FDA 510(k) clearance on 1991-12-04, under 510(k) number K913520.
Who is the listed applicant for EVACU SLED?
The FDA 510(k) record lists Nexus Health Care Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EVACU SLED?
The FDA product code for EVACU SLED is FPP.
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.
Related Devices (Code: FPP)
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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