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FDA 510(k)

MEDIGAS SUCTION/DRAINAGE EQUIPMENT

K-Number: K821841 · 1982-07-02

Decision Date1982-07-02
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDIGAS SUCTION/DRAINAGE EQUIPMENT is the device name listed in this FDA 510(k) record. The listed applicant is Linde Div. Union Carbide Corp.. It received FDA 510(k) clearance on 1982-07-02 under 510(k) number K821841. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIGAS SUCTION/DRAINAGE EQUIPMENT?

MEDIGAS SUCTION/DRAINAGE EQUIPMENT is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Linde Div. Union Carbide Corp.. The 510(k) number is K821841.

When did MEDIGAS SUCTION/DRAINAGE EQUIPMENT receive FDA 510(k) clearance?

MEDIGAS SUCTION/DRAINAGE EQUIPMENT received FDA 510(k) clearance on 1982-07-02, under 510(k) number K821841.

Who is the listed applicant for MEDIGAS SUCTION/DRAINAGE EQUIPMENT?

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

What is the FDA product code for MEDIGAS SUCTION/DRAINAGE EQUIPMENT?

The FDA product code for MEDIGAS SUCTION/DRAINAGE EQUIPMENT is GCX.

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 Linde Div. Union Carbide 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.

Related Devices (Code: GCX)

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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