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FDA 510(k)

EASYCELL CELL LOCATOR

K-Number: K092116 · 2010-05-12

ApplicantMedica Corp.
Decision Date2010-05-12
Product CodeJOY
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

EASYCELL CELL LOCATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medica Corp.. It received FDA 510(k) clearance on 2010-05-12 under 510(k) number K092116. The device is classified under product code JOY. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYCELL CELL LOCATOR?

EASYCELL CELL LOCATOR is a medical device that received FDA 510(k) clearance on 2010-05-12. The listed applicant is Medica Corp.. The 510(k) number is K092116.

When did EASYCELL CELL LOCATOR receive FDA 510(k) clearance?

EASYCELL CELL LOCATOR received FDA 510(k) clearance on 2010-05-12, under 510(k) number K092116.

Who is the listed applicant for EASYCELL CELL LOCATOR?

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

What is the FDA product code for EASYCELL CELL LOCATOR?

The FDA product code for EASYCELL CELL LOCATOR is JOY.

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 Medica Corp. 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 47 devices →

Related Devices (Code: JOY)

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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