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FDA 510(k)

OHIO THORACIC SUCTION REGULATOR

K-Number: K802285 · 1980-10-03

ApplicantOhio Medical Products
Decision Date1980-10-03
Product CodeKOP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OHIO THORACIC SUCTION REGULATOR 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 1980-10-03 under 510(k) number K802285. The device is classified under product code KOP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHIO THORACIC SUCTION REGULATOR?

OHIO THORACIC SUCTION REGULATOR is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Ohio Medical Products. The 510(k) number is K802285.

When did OHIO THORACIC SUCTION REGULATOR receive FDA 510(k) clearance?

OHIO THORACIC SUCTION REGULATOR received FDA 510(k) clearance on 1980-10-03, under 510(k) number K802285.

Who is the listed applicant for OHIO THORACIC SUCTION REGULATOR?

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 SUCTION REGULATOR?

The FDA product code for OHIO THORACIC SUCTION REGULATOR is KOP.

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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.

K841733OHIO WASTE GAS SCAVENGING RESERVOIRK842003OHIO WASTE GAS SCAVENGING INTERFACEK840356OHIO UNITROL II ANESTHESIA GAS MACHINEK841274BAG-TO-VENTILATOR SELECTOR VALVEK840967OHIO HEAT REFLECTING PATCHK840857OHIO 3000 INFANT WARMER SYSTEM

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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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