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FDA 510(k)

IRRIVAGE

K-Number: K922785 · 1992-10-16

ApplicantAutovage
Decision Date1992-10-16
Product CodeEYF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IRRIVAGE is the device name listed in this FDA 510(k) record. The listed applicant is Autovage. It received FDA 510(k) clearance on 1992-10-16 under 510(k) number K922785. The device is classified under product code EYF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IRRIVAGE?

IRRIVAGE is a medical device that received FDA 510(k) clearance on 1992-10-16. The listed applicant is Autovage. The 510(k) number is K922785.

When did IRRIVAGE receive FDA 510(k) clearance?

IRRIVAGE received FDA 510(k) clearance on 1992-10-16, under 510(k) number K922785.

Who is the listed applicant for IRRIVAGE?

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

What is the FDA product code for IRRIVAGE?

The FDA product code for IRRIVAGE is EYF.

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 Autovage 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 7 devices →

Related Devices (Code: EYF)

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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