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FDA 510(k)

ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER

K-Number: K973938 · 1998-02-04

ApplicantSfri, Inc.
Decision Date1998-02-04
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER is the device name listed in this FDA 510(k) record. The listed applicant is Sfri, Inc.. It received FDA 510(k) clearance on 1998-02-04 under 510(k) number K973938. 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 ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER?

ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER is a medical device that received FDA 510(k) clearance on 1998-02-04. The listed applicant is Sfri, Inc.. The 510(k) number is K973938.

When did ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER receive FDA 510(k) clearance?

ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER received FDA 510(k) clearance on 1998-02-04, under 510(k) number K973938.

Who is the listed applicant for ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER?

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

What is the FDA product code for ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READER?

The FDA product code for ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND 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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, Inc.K962166ORIGEN ANALYZERIgen, Inc.

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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