SURVIVAL KIT, INDIVIDUAL
K-Number: K871437 · 1987-07-09
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Device Summary
Frequently Asked Questions
What is the SURVIVAL KIT, INDIVIDUAL?
SURVIVAL KIT, INDIVIDUAL is a medical device that received FDA 510(k) clearance on 1987-07-09. The listed applicant is Fraass Survival Systems, Inc.. The 510(k) number is K871437.
When did SURVIVAL KIT, INDIVIDUAL receive FDA 510(k) clearance?
SURVIVAL KIT, INDIVIDUAL received FDA 510(k) clearance on 1987-07-09, under 510(k) number K871437.
Who is the listed applicant for SURVIVAL KIT, INDIVIDUAL?
The FDA 510(k) record lists Fraass Survival Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURVIVAL KIT, INDIVIDUAL?
The FDA product code for SURVIVAL KIT, INDIVIDUAL is LRO.
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 Fraass Survival Systems, 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: LRO)
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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