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FDA 510(k)

PICASSO MASTER, ECT AND MASTER 3D

K-Number: K081847 · 2008-08-21

ApplicantE-Woo Technology
Decision Date2008-08-21
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PICASSO MASTER, ECT AND MASTER 3D is the device name listed in this FDA 510(k) record. The listed applicant is E-Woo Technology. It received FDA 510(k) clearance on 2008-08-21 under 510(k) number K081847. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PICASSO MASTER, ECT AND MASTER 3D?

PICASSO MASTER, ECT AND MASTER 3D is a medical device that received FDA 510(k) clearance on 2008-08-21. The listed applicant is E-Woo Technology. The 510(k) number is K081847.

When did PICASSO MASTER, ECT AND MASTER 3D receive FDA 510(k) clearance?

PICASSO MASTER, ECT AND MASTER 3D received FDA 510(k) clearance on 2008-08-21, under 510(k) number K081847.

Who is the listed applicant for PICASSO MASTER, ECT AND MASTER 3D?

The FDA 510(k) record lists E-Woo Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PICASSO MASTER, ECT AND MASTER 3D?

The FDA product code for PICASSO MASTER, ECT AND MASTER 3D is JAK.

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Other records listing E-Woo Technology as applicant

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Related Devices (Code: JAK)

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

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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