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FDA 510(k)

COLOSTOMY DEVICE, MACLET MAGNETIC

K-Number: K782154 · 1979-06-21

ApplicantMaclet Medical Devices, Inc.
Decision Date1979-06-21
Product Code
DecisionSubstantially Equivalent

Device Summary

COLOSTOMY DEVICE, MACLET MAGNETIC is the device name listed in this FDA 510(k) record. The listed applicant is Maclet Medical Devices, Inc.. It received FDA 510(k) clearance on 1979-06-21 under 510(k) number K782154. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLOSTOMY DEVICE, MACLET MAGNETIC?

COLOSTOMY DEVICE, MACLET MAGNETIC is a medical device that received FDA 510(k) clearance on 1979-06-21. The listed applicant is Maclet Medical Devices, Inc.. The 510(k) number is K782154.

When did COLOSTOMY DEVICE, MACLET MAGNETIC receive FDA 510(k) clearance?

COLOSTOMY DEVICE, MACLET MAGNETIC received FDA 510(k) clearance on 1979-06-21, under 510(k) number K782154.

Who is the listed applicant for COLOSTOMY DEVICE, MACLET MAGNETIC?

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

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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.

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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.

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