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FDA 510(k)

ANTHOS 2010 READER

K-Number: K955077 · 1995-12-04

ApplicantAnthos Labtec, Inc.
Decision Date1995-12-04
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANTHOS 2010 READER is the device name listed in this FDA 510(k) record. The listed applicant is Anthos Labtec, Inc.. It received FDA 510(k) clearance on 1995-12-04 under 510(k) number K955077. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTHOS 2010 READER?

ANTHOS 2010 READER is a medical device that received FDA 510(k) clearance on 1995-12-04. The listed applicant is Anthos Labtec, Inc.. The 510(k) number is K955077.

When did ANTHOS 2010 READER receive FDA 510(k) clearance?

ANTHOS 2010 READER received FDA 510(k) clearance on 1995-12-04, under 510(k) number K955077.

Who is the listed applicant for ANTHOS 2010 READER?

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

What is the FDA product code for ANTHOS 2010 READER?

The FDA product code for ANTHOS 2010 READER is JJQ.

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Related Devices (Code: JJQ)

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

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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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