Boehringer Mannheim Es 300 Al(Autoloader) Analyzer

FDA 510(k) K932778 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK932778

Submission

Device name
Boehringer Mannheim Es 300 Al(Autoloader) Analyzer
Applicant
Boehringer Mannheim Corp.
Indianapolis, IN, US
Received
June 8, 1993
Decision date
November 17, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JJQ – Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2300
Specialty
Clinical Chemistry

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K955077Anthos 2010 ReaderJJQ · Traditional Anthos Labtec, Inc.12/04/1995SE
K953710ELX808 Automated Microplate ReadersJJQ · Traditional Bio-Tek Instruments, Inc.10/25/1995SE
K953572ELX800UVJJQ · Traditional Bio-Tek Instruments, Inc.10/19/1995SE

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K983469Preciset Serum Proteins CalibratorJIX · Traditional 11/25/1998SE
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Questions and answers

When was Boehringer Mannheim Es 300 Al(Autoloader) Analyzer cleared by the FDA?

Boehringer Mannheim Es 300 Al(Autoloader) Analyzer (K932778) received a 510(k) decision of Substantially Equivalent on November 17, 1993, 162 days after the submission was received.

What is the product code of K932778?

The FDA product code is JJQ – Colorimeter, Photometer, Spectrophotometer For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2300.