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FDA 510(k)

DUAL INCU I

K-Number: K102226 · 2011-01-04

Decision Date2011-01-04
Product CodeFMZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUAL INCU I is the device name listed in this FDA 510(k) record. The listed applicant is Atom Medical Corporation. It received FDA 510(k) clearance on 2011-01-04 under 510(k) number K102226. The device is classified under product code FMZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL INCU I?

DUAL INCU I is a medical device that received FDA 510(k) clearance on 2011-01-04. The listed applicant is Atom Medical Corporation. The 510(k) number is K102226.

When did DUAL INCU I receive FDA 510(k) clearance?

DUAL INCU I received FDA 510(k) clearance on 2011-01-04, under 510(k) number K102226.

Who is the listed applicant for DUAL INCU I?

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

What is the FDA product code for DUAL INCU I?

The FDA product code for DUAL INCU I is FMZ.

Other records listing Atom Medical Corporation 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 10 devices →

Related Devices (Code: FMZ)

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

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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