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FDA 510(k)

DMI SERIES 90 EXAMINATION TABLE

K-Number: K894788 · 1989-09-08

ApplicantM.D. Intl., Inc.
Decision Date1989-09-08
Product CodeKMN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DMI SERIES 90 EXAMINATION TABLE is the device name listed in this FDA 510(k) record. The listed applicant is M.D. Intl., Inc.. It received FDA 510(k) clearance on 1989-09-08 under 510(k) number K894788. The device is classified under product code KMN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMI SERIES 90 EXAMINATION TABLE?

DMI SERIES 90 EXAMINATION TABLE is a medical device that received FDA 510(k) clearance on 1989-09-08. The listed applicant is M.D. Intl., Inc.. The 510(k) number is K894788.

When did DMI SERIES 90 EXAMINATION TABLE receive FDA 510(k) clearance?

DMI SERIES 90 EXAMINATION TABLE received FDA 510(k) clearance on 1989-09-08, under 510(k) number K894788.

Who is the listed applicant for DMI SERIES 90 EXAMINATION TABLE?

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

What is the FDA product code for DMI SERIES 90 EXAMINATION TABLE?

The FDA product code for DMI SERIES 90 EXAMINATION TABLE is KMN.

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Other records listing M.D. Intl., 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.

K894789DMI 250 SERIES POWER SURGERY TABLEK870832OXY-THERMK771249JOY LIGHT

Related Devices (Code: KMN)

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.

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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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