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FDA 510(k)

SECURITY STRETCH BRIEF-MEDICAL

K-Number: K833245 · 1983-10-31

Decision Date1983-10-31
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SECURITY STRETCH BRIEF-MEDICAL is the device name listed in this FDA 510(k) record. The listed applicant is Mb Products, Ltd.. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K833245. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECURITY STRETCH BRIEF-MEDICAL?

SECURITY STRETCH BRIEF-MEDICAL is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Mb Products, Ltd.. The 510(k) number is K833245.

When did SECURITY STRETCH BRIEF-MEDICAL receive FDA 510(k) clearance?

SECURITY STRETCH BRIEF-MEDICAL received FDA 510(k) clearance on 1983-10-31, under 510(k) number K833245.

Who is the listed applicant for SECURITY STRETCH BRIEF-MEDICAL?

The FDA 510(k) record lists Mb Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SECURITY STRETCH BRIEF-MEDICAL?

The FDA product code for SECURITY STRETCH BRIEF-MEDICAL is KNX.

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: KNX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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