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FDA 510(k)

AUDIT MICROCV RF/CRP LINEARITY SET

K-Number: K101226 · 2010-08-31

Decision Date2010-08-31
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUDIT MICROCV RF/CRP LINEARITY SET is the device name listed in this FDA 510(k) record. The listed applicant is Aalto Scientific, Ltd.. It received FDA 510(k) clearance on 2010-08-31 under 510(k) number K101226. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUDIT MICROCV RF/CRP LINEARITY SET?

AUDIT MICROCV RF/CRP LINEARITY SET is a medical device that received FDA 510(k) clearance on 2010-08-31. The listed applicant is Aalto Scientific, Ltd.. The 510(k) number is K101226.

When did AUDIT MICROCV RF/CRP LINEARITY SET receive FDA 510(k) clearance?

AUDIT MICROCV RF/CRP LINEARITY SET received FDA 510(k) clearance on 2010-08-31, under 510(k) number K101226.

Who is the listed applicant for AUDIT MICROCV RF/CRP LINEARITY SET?

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

What is the FDA product code for AUDIT MICROCV RF/CRP LINEARITY SET?

The FDA product code for AUDIT MICROCV RF/CRP LINEARITY SET is JJY.

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 Aalto Scientific, 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 31 devices →

Related Devices (Code: JJY)

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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