HAND-CARRIED STRETCHERS
K-Number: K904494 · 1990-10-12
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Device Summary
Frequently Asked Questions
What is the HAND-CARRIED STRETCHERS?
HAND-CARRIED STRETCHERS is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is Minto Research & Development, Inc.. The 510(k) number is K904494.
When did HAND-CARRIED STRETCHERS receive FDA 510(k) clearance?
HAND-CARRIED STRETCHERS received FDA 510(k) clearance on 1990-10-12, under 510(k) number K904494.
Who is the listed applicant for HAND-CARRIED STRETCHERS?
The FDA 510(k) record lists Minto Research & Development, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HAND-CARRIED STRETCHERS?
The FDA product code for HAND-CARRIED STRETCHERS 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.
Other records listing Minto Research & Development, 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: 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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