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FDA 510(k)

MINIVAGE(R)

K-Number: K911919 · 1991-07-26

ApplicantAutovage
Decision Date1991-07-26
Product CodeKDH
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MINIVAGE(R) is the device name listed in this FDA 510(k) record. The listed applicant is Autovage. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K911919. The device is classified under product code KDH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIVAGE(R)?

MINIVAGE(R) is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Autovage. The 510(k) number is K911919.

When did MINIVAGE(R) receive FDA 510(k) clearance?

MINIVAGE(R) received FDA 510(k) clearance on 1991-07-26, under 510(k) number K911919.

Who is the listed applicant for MINIVAGE(R)?

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 MINIVAGE(R)?

The FDA product code for MINIVAGE(R) is KDH.

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.

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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.

K922785IRRIVAGEK914908QUICVAGE PLUSK914907QUICVAGEK911788ECONOVAGE RK840943ENDO-JECTK823195GASTRIC LAVAGE KIT

View all 7 devices →

Related Devices (Code: KDH)

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.

K983624GILTECH PLUS CONNECTING TUBE SETGiltech Plus, Inc.K981286SUPERFLOW IRRIGATION AND ASPIRATION TUBING SETSArmm, Inc.K971259COMBIPORT FLUID LAVAGE DEVICEB.Braun Medical, Inc.K962850TUM-E-VACEthox Corp.K951533EASI-LAV PEDIATRIC / ADULT GASTRIC LAVAGE KITBallard Medical ProductsK923497FLUSHING IRRIGATION SETOrion Life Systems, Inc.

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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