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FDA 510(k)

OHMEDA DOUBLE SWIVEL ADAPTER

K-Number: K844656 · 1985-02-12

Decision Date1985-02-12
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHMEDA DOUBLE SWIVEL ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1985-02-12 under 510(k) number K844656. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA DOUBLE SWIVEL ADAPTER?

OHMEDA DOUBLE SWIVEL ADAPTER is a medical device that received FDA 510(k) clearance on 1985-02-12. The listed applicant is Ohmeda Medical. The 510(k) number is K844656.

When did OHMEDA DOUBLE SWIVEL ADAPTER receive FDA 510(k) clearance?

OHMEDA DOUBLE SWIVEL ADAPTER received FDA 510(k) clearance on 1985-02-12, under 510(k) number K844656.

Who is the listed applicant for OHMEDA DOUBLE SWIVEL ADAPTER?

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 DOUBLE SWIVEL ADAPTER?

The FDA product code for OHMEDA DOUBLE SWIVEL ADAPTER is BZA.

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: BZA)

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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