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FDA 510(k)

OHMEDA 7800 ANESTHESIA VENTILATOR

K-Number: K913791 · 1993-04-08

Decision Date1993-04-08
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHMEDA 7800 ANESTHESIA VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Anesthesia Systems Therapy Group. It received FDA 510(k) clearance on 1993-04-08 under 510(k) number K913791. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA 7800 ANESTHESIA VENTILATOR?

OHMEDA 7800 ANESTHESIA VENTILATOR is a medical device that received FDA 510(k) clearance on 1993-04-08. The listed applicant is Ohmeda Anesthesia Systems Therapy Group. The 510(k) number is K913791.

When did OHMEDA 7800 ANESTHESIA VENTILATOR receive FDA 510(k) clearance?

OHMEDA 7800 ANESTHESIA VENTILATOR received FDA 510(k) clearance on 1993-04-08, under 510(k) number K913791.

Who is the listed applicant for OHMEDA 7800 ANESTHESIA VENTILATOR?

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

What is the FDA product code for OHMEDA 7800 ANESTHESIA VENTILATOR?

The FDA product code for OHMEDA 7800 ANESTHESIA VENTILATOR is BSZ.

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 Anesthesia Systems Therapy Group 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: BSZ)

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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