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FDA 510(k)

MIDMARK MAGNUM GENERAL SURGICAL TABLE

K-Number: K934744 · 1994-03-28

ApplicantMidmark Corp.
Decision Date1994-03-28
Product CodeGDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MIDMARK MAGNUM GENERAL SURGICAL TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1994-03-28 under 510(k) number K934744. The device is classified under product code GDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDMARK MAGNUM GENERAL SURGICAL TABLE?

MIDMARK MAGNUM GENERAL SURGICAL TABLE is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Midmark Corp.. The 510(k) number is K934744.

When did MIDMARK MAGNUM GENERAL SURGICAL TABLE receive FDA 510(k) clearance?

MIDMARK MAGNUM GENERAL SURGICAL TABLE received FDA 510(k) clearance on 1994-03-28, under 510(k) number K934744.

Who is the listed applicant for MIDMARK MAGNUM GENERAL SURGICAL TABLE?

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

What is the FDA product code for MIDMARK MAGNUM GENERAL SURGICAL TABLE?

The FDA product code for MIDMARK MAGNUM GENERAL SURGICAL TABLE is GDC.

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 Midmark Corp. 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 31 devices →

Related Devices (Code: GDC)

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

View on FDA Database →

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

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