Titertek-Enterobac Rapid Automated

FDA 510(k) K842182 · Flow Laboratories, Inc.

Unknown

510(k) numberK842182

Submission

Device name
Titertek-Enterobac Rapid Automated
Applicant
Flow Laboratories, Inc.
Mchenry, IL, US
Received
June 1, 1984
Decision date
June 1, 1984
Decision
Unknown (SESP)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

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Questions and answers

When was Titertek-Enterobac Rapid Automated cleared by the FDA?

Titertek-Enterobac Rapid Automated (K842182) received a 510(k) decision of Unknown on June 1, 1984, 0 days after the submission was received.