FDA 510(k)

BARD URINE COLLECTION PRODUCTS MODIFICATION

K-Number: K940206 · 1994-09-16

Decision Date1994-09-16

Product CodeKNX

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BARD URINE COLLECTION PRODUCTS MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1994-09-16 under 510(k) number K940206. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD URINE COLLECTION PRODUCTS MODIFICATION?

BARD URINE COLLECTION PRODUCTS MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-09-16. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K940206.

When did BARD URINE COLLECTION PRODUCTS MODIFICATION receive FDA 510(k) clearance?

BARD URINE COLLECTION PRODUCTS MODIFICATION received FDA 510(k) clearance on 1994-09-16, under 510(k) number K940206.

Who is the listed applicant for BARD URINE COLLECTION PRODUCTS MODIFICATION?

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

What is the FDA product code for BARD URINE COLLECTION PRODUCTS MODIFICATION?

The FDA product code for BARD URINE COLLECTION PRODUCTS MODIFICATION is KNX.

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Related Devices (Code: KNX)

K110518IBAGFuture Path Medical, LLC K9733644L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAGMaersk Medical A/S K972887MEDLINE PREMIUM LEG BAG, MEDLINE FABRIC BAC LEG BAG, MEDLINE URINARY LEG BAGMedline Industries, Inc.K971271BESECURE EXTERNAL URINARY COLLECTION SYSTEMUrology Research Intl., Inc.K971929AMSINO URINARY LEG BAGAmsino Intl., Inc.K971764WELCON HUE-VU URINARY DRAINAGE BAGWelcon, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.