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FDA 510(k)

OHMEDA POSI-PULSE SUCTION UNIT

K-Number: K861261 · 1986-05-30

Decision Date1986-05-30
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OHMEDA POSI-PULSE SUCTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1986-05-30 under 510(k) number K861261. 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 OHMEDA POSI-PULSE SUCTION UNIT?

OHMEDA POSI-PULSE SUCTION UNIT is a medical device that received FDA 510(k) clearance on 1986-05-30. The listed applicant is Ohmeda Medical. The 510(k) number is K861261.

When did OHMEDA POSI-PULSE SUCTION UNIT receive FDA 510(k) clearance?

OHMEDA POSI-PULSE SUCTION UNIT received FDA 510(k) clearance on 1986-05-30, under 510(k) number K861261.

Who is the listed applicant for OHMEDA POSI-PULSE SUCTION UNIT?

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

What is the FDA product code for OHMEDA POSI-PULSE SUCTION UNIT?

The FDA product code for OHMEDA POSI-PULSE SUCTION 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 Ohmeda Medical 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 119 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

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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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