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FDA 510(k)

MEDCO MEMORY RETRACTOR SYSTEM

K-Number: K874829 · 1988-03-24

Decision Date1988-03-24
Product CodeGZT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDCO MEMORY RETRACTOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Development Co., Inc.. It received FDA 510(k) clearance on 1988-03-24 under 510(k) number K874829. The device is classified under product code GZT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCO MEMORY RETRACTOR SYSTEM?

MEDCO MEMORY RETRACTOR SYSTEM is a medical device that received FDA 510(k) clearance on 1988-03-24. The listed applicant is Medical Equipment Development Co., Inc.. The 510(k) number is K874829.

When did MEDCO MEMORY RETRACTOR SYSTEM receive FDA 510(k) clearance?

MEDCO MEMORY RETRACTOR SYSTEM received FDA 510(k) clearance on 1988-03-24, under 510(k) number K874829.

Who is the listed applicant for MEDCO MEMORY RETRACTOR SYSTEM?

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

What is the FDA product code for MEDCO MEMORY RETRACTOR SYSTEM?

The FDA product code for MEDCO MEMORY RETRACTOR SYSTEM is GZT.

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 Equipment Development Co., 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.

View all 7 devices →

Related Devices (Code: GZT)

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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