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FDA 510(k)

ECOTABS

K-Number: K950587 · 1995-10-16

ApplicantMsb , Ltd.
Decision Date1995-10-16
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ECOTABS is the device name listed in this FDA 510(k) record. The listed applicant is Msb , Ltd.. It received FDA 510(k) clearance on 1995-10-16 under 510(k) number K950587. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECOTABS?

ECOTABS is a medical device that received FDA 510(k) clearance on 1995-10-16. The listed applicant is Msb , Ltd.. The 510(k) number is K950587.

When did ECOTABS receive FDA 510(k) clearance?

ECOTABS received FDA 510(k) clearance on 1995-10-16, under 510(k) number K950587.

Who is the listed applicant for ECOTABS?

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

What is the FDA product code for ECOTABS?

The FDA product code for ECOTABS is DRX.

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 Msb , Ltd. 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.

View all 7 devices →

Related Devices (Code: DRX)

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.

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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