VACUUM STRETCHER IMMOBILIZER
K-Number: K840034 · 1984-02-27
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Device Summary
Frequently Asked Questions
What is the VACUUM STRETCHER IMMOBILIZER?
VACUUM STRETCHER IMMOBILIZER is a medical device that received FDA 510(k) clearance on 1984-02-27. The listed applicant is Medicon, Inc.. The 510(k) number is K840034.
When did VACUUM STRETCHER IMMOBILIZER receive FDA 510(k) clearance?
VACUUM STRETCHER IMMOBILIZER received FDA 510(k) clearance on 1984-02-27, under 510(k) number K840034.
Who is the listed applicant for VACUUM STRETCHER IMMOBILIZER?
The FDA 510(k) record lists Medicon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VACUUM STRETCHER IMMOBILIZER?
The FDA product code for VACUUM STRETCHER IMMOBILIZER 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 Medicon, 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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