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FDA 510(k)

MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE

K-Number: K924002 · 1992-11-09

Decision Date1992-11-09
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE is the device name listed in this FDA 510(k) record. The listed applicant is Midland Mfg. Co.. It received FDA 510(k) clearance on 1992-11-09 under 510(k) number K924002. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE?

MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE is a medical device that received FDA 510(k) clearance on 1992-11-09. The listed applicant is Midland Mfg. Co.. The 510(k) number is K924002.

When did MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE receive FDA 510(k) clearance?

MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE received FDA 510(k) clearance on 1992-11-09, under 510(k) number K924002.

Who is the listed applicant for MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE?

The FDA 510(k) record lists Midland Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE?

The FDA product code for MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE is INQ.

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 Midland Mfg. Co. 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: INQ)

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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