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FDA 510(k)

MINIMUFFS

K-Number: K935160 · 1995-02-09

Decision Date1995-02-09
Product CodeEWE
DecisionSubstantially Equivalent

Device Summary

MINIMUFFS is the device name listed in this FDA 510(k) record. The listed applicant is Natus Medical, Inc.. It received FDA 510(k) clearance on 1995-02-09 under 510(k) number K935160. The device is classified under product code EWE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIMUFFS?

MINIMUFFS is a medical device that received FDA 510(k) clearance on 1995-02-09. The listed applicant is Natus Medical, Inc.. The 510(k) number is K935160.

When did MINIMUFFS receive FDA 510(k) clearance?

MINIMUFFS received FDA 510(k) clearance on 1995-02-09, under 510(k) number K935160.

Who is the listed applicant for MINIMUFFS?

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

What is the FDA product code for MINIMUFFS?

The FDA product code for MINIMUFFS is EWE.

Related Clinical Trials

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.

Other records listing Natus Medical, Inc. 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.

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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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