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FDA 510(k)

DYNA-FLO URINARY DRAINAGE BAG

K-Number: K896695 · 1990-05-02

ApplicantMedline Industries, Inc.
Decision Date1990-05-02
Product CodeEYZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DYNA-FLO URINARY DRAINAGE BAG is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1990-05-02 under 510(k) number K896695. The device is classified under product code EYZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNA-FLO URINARY DRAINAGE BAG?

DYNA-FLO URINARY DRAINAGE BAG is a medical device that received FDA 510(k) clearance on 1990-05-02. The listed applicant is Medline Industries, Inc.. The 510(k) number is K896695.

When did DYNA-FLO URINARY DRAINAGE BAG receive FDA 510(k) clearance?

DYNA-FLO URINARY DRAINAGE BAG received FDA 510(k) clearance on 1990-05-02, under 510(k) number K896695.

Who is the listed applicant for DYNA-FLO URINARY DRAINAGE BAG?

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

What is the FDA product code for DYNA-FLO URINARY DRAINAGE BAG?

The FDA product code for DYNA-FLO URINARY DRAINAGE BAG is EYZ.

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Other records listing Medline Industries, Inc. as applicant

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Related Devices (Code: EYZ)

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.

K964219ZIP CONDOM CATHETERGoulter Medical, Inc.K961906UNI-GARD QUIK CATH(SIZES 8 FRENCH THROUGH 18)UG 10008,10010,10012,10014,10016,10018Spectrum Medsystems Corp.K952780URINARY GEL DRAINAGE SYSTEMP.A.M., Inc.K951597URINARY DRAINAGE BAGKey Medical Services, Inc.K942753ONE STEP SPECIMEN COLLECTOR/TRANSPORT CONTAINERResearched, Novel Medical Devices (Rn/Md)K933126COMFORTCARE SYSTEMPatsy J. Trisler, J.D.

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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