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FDA 510(k)

QUICVAGE PLUS

K-Number: K914908 · 1992-04-13

ApplicantAutovage
Decision Date1992-04-13
Product CodeKDH
Advisory CommitteeGU
DecisionUnknown

Device Summary

QUICVAGE PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Autovage. It received FDA 510(k) clearance on 1992-04-13 under 510(k) number K914908. The device is classified under product code KDH. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the QUICVAGE PLUS?

QUICVAGE PLUS is a medical device that received FDA 510(k) clearance on 1992-04-13. The listed applicant is Autovage. The 510(k) number is K914908.

When did QUICVAGE PLUS receive FDA 510(k) clearance?

QUICVAGE PLUS received FDA 510(k) clearance on 1992-04-13, under 510(k) number K914908.

Who is the listed applicant for QUICVAGE PLUS?

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 QUICVAGE PLUS?

The FDA product code for QUICVAGE PLUS is KDH.

Related Clinical Trials

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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.

K922785IRRIVAGEK914907QUICVAGEK911919MINIVAGE(R)K911788ECONOVAGE 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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