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FDA 510(k)

OHMEDA 7900 ANESTHESIA VENTILATOR

K-Number: K960964 · 1996-09-27

Decision Date1996-09-27
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

OHMEDA 7900 ANESTHESIA VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1996-09-27 under 510(k) number K960964. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the OHMEDA 7900 ANESTHESIA VENTILATOR?

OHMEDA 7900 ANESTHESIA VENTILATOR is a medical device that received FDA 510(k) clearance on 1996-09-27. The listed applicant is Ohmeda Medical. The 510(k) number is K960964.

When did OHMEDA 7900 ANESTHESIA VENTILATOR receive FDA 510(k) clearance?

OHMEDA 7900 ANESTHESIA VENTILATOR received FDA 510(k) clearance on 1996-09-27, under 510(k) number K960964.

Who is the listed applicant for OHMEDA 7900 ANESTHESIA VENTILATOR?

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 7900 ANESTHESIA VENTILATOR?

The FDA product code for OHMEDA 7900 ANESTHESIA VENTILATOR is CBK.

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: CBK)

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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