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FDA 510(k)

ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III

K-Number: K931907 · 1993-09-29

ApplicantAnthos Labtec Instruments
Decision Date1993-09-29
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III is the device name listed in this FDA 510(k) record. The listed applicant is Anthos Labtec Instruments. It received FDA 510(k) clearance on 1993-09-29 under 510(k) number K931907. 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 HT READERS, INCLUDING THE ANTHOS HT II&III?

ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III is a medical device that received FDA 510(k) clearance on 1993-09-29. The listed applicant is Anthos Labtec Instruments. The 510(k) number is K931907.

When did ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III receive FDA 510(k) clearance?

ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III received FDA 510(k) clearance on 1993-09-29, under 510(k) number K931907.

Who is the listed applicant for ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III?

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

What is the FDA product code for ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III?

The FDA product code for ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III is JJQ.

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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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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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, Inc.

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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