FORCEGUARD
K-Number: K955034 · 1996-04-10
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Device Summary
Frequently Asked Questions
What is the FORCEGUARD?
FORCEGUARD is a medical device that received FDA 510(k) clearance on 1996-04-10. The listed applicant is Impact Monitors, Inc.. The 510(k) number is K955034.
When did FORCEGUARD receive FDA 510(k) clearance?
FORCEGUARD received FDA 510(k) clearance on 1996-04-10, under 510(k) number K955034.
Who is the listed applicant for FORCEGUARD?
The FDA 510(k) record lists Impact Monitors, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORCEGUARD?
The FDA product code for FORCEGUARD is IRN.
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: IRN)
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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