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FDA 510(k)

CATHETER, MMG LATEX EXTERNAL

K-Number: K790279 · 1979-03-06

ApplicantMedical Marketing Group
Decision Date1979-03-06
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER, MMG LATEX EXTERNAL is the device name listed in this FDA 510(k) record. The listed applicant is Medical Marketing Group. It received FDA 510(k) clearance on 1979-03-06 under 510(k) number K790279. 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 CATHETER, MMG LATEX EXTERNAL?

CATHETER, MMG LATEX EXTERNAL is a medical device that received FDA 510(k) clearance on 1979-03-06. The listed applicant is Medical Marketing Group. The 510(k) number is K790279.

When did CATHETER, MMG LATEX EXTERNAL receive FDA 510(k) clearance?

CATHETER, MMG LATEX EXTERNAL received FDA 510(k) clearance on 1979-03-06, under 510(k) number K790279.

Who is the listed applicant for CATHETER, MMG LATEX EXTERNAL?

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

What is the FDA product code for CATHETER, MMG LATEX EXTERNAL?

The FDA product code for CATHETER, MMG LATEX EXTERNAL is KNX.

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Other records listing Medical Marketing Group 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.

K910022MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KITK884819O'NEIL URINARY CATHETER INTRODUCERK874682MMG CATHETER PLUG W/DRAINAGE TUBE COVERK871999MMG URO-SELF CATHETERK863912THE MMG 5 IN 1 CONNECTORK840838MMG CONNECTIVE TUBING

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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, LLCK9733644L DRAINAGE BAG, 4L BAG FOR PERITONEAL DIALYSIS, 4L URINARY DRAINAGE BAGMaersk Medical A/SK972887MEDLINE 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

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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