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FDA 510(k)

MEC-1 VIDEO COMBO SYSTEM

K-Number: K883944 · 1988-09-28

Decision Date1988-09-28
Product CodeFTS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEC-1 VIDEO COMBO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Concepts, Inc.. It received FDA 510(k) clearance on 1988-09-28 under 510(k) number K883944. The device is classified under product code FTS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEC-1 VIDEO COMBO SYSTEM?

MEC-1 VIDEO COMBO SYSTEM is a medical device that received FDA 510(k) clearance on 1988-09-28. The listed applicant is Medical Concepts, Inc.. The 510(k) number is K883944.

When did MEC-1 VIDEO COMBO SYSTEM receive FDA 510(k) clearance?

MEC-1 VIDEO COMBO SYSTEM received FDA 510(k) clearance on 1988-09-28, under 510(k) number K883944.

Who is the listed applicant for MEC-1 VIDEO COMBO SYSTEM?

The FDA 510(k) record lists Medical Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEC-1 VIDEO COMBO SYSTEM?

The FDA product code for MEC-1 VIDEO COMBO SYSTEM is FTS.

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 Medical Concepts, 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: FTS)

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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