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FDA 510(k)

EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000

K-Number: K873489 · 1987-12-29

Decision Date1987-12-29
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000 is the device name listed in this FDA 510(k) record. The listed applicant is J. H. Emerson Co.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K873489. 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 EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000?

EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000 is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is J. H. Emerson Co.. The 510(k) number is K873489.

When did EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000 receive FDA 510(k) clearance?

EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000 received FDA 510(k) clearance on 1987-12-29, under 510(k) number K873489.

Who is the listed applicant for EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000?

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

What is the FDA product code for EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000?

The FDA product code for EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000 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 J. H. Emerson 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.

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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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