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FDA 510(k)

OHIO THORACIC COLLECTION UNIT

K-Number: K801942 · 1980-09-16

Decision Date1980-09-16
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OHIO THORACIC COLLECTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Ohio Medical Products. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K801942. 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 OHIO THORACIC COLLECTION UNIT?

OHIO THORACIC COLLECTION UNIT is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Ohio Medical Products. The 510(k) number is K801942.

When did OHIO THORACIC COLLECTION UNIT receive FDA 510(k) clearance?

OHIO THORACIC COLLECTION UNIT received FDA 510(k) clearance on 1980-09-16, under 510(k) number K801942.

Who is the listed applicant for OHIO THORACIC COLLECTION UNIT?

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

What is the FDA product code for OHIO THORACIC COLLECTION UNIT?

The FDA product code for OHIO THORACIC COLLECTION UNIT 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 Ohio Medical Products 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 47 devices →

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

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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