FDA 510(k)

LOGO-NU-WAY

K-Number: K800186 · 1980-02-26

Decision Date1980-02-26

Product CodeKNX

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

LOGO-NU-WAY is the device name listed in this FDA 510(k) record. The listed applicant is Gary Giancarlo. It received FDA 510(k) clearance on 1980-02-26 under 510(k) number K800186. 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 LOGO-NU-WAY?

LOGO-NU-WAY is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Gary Giancarlo. The 510(k) number is K800186.

When did LOGO-NU-WAY receive FDA 510(k) clearance?

LOGO-NU-WAY received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800186.

Who is the listed applicant for LOGO-NU-WAY?

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

What is the FDA product code for LOGO-NU-WAY?

The FDA product code for LOGO-NU-WAY is KNX.

Related Devices (Code: KNX)

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.

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.