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FDA 510(k)

AUTOMATED WORKCELL CONTROL SOFTWARE

K-Number: K010500 · 2001-08-01

ApplicantLab-Interlink, Inc.
Decision Date2001-08-01
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTOMATED WORKCELL CONTROL SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Lab-Interlink, Inc.. It received FDA 510(k) clearance on 2001-08-01 under 510(k) number K010500. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATED WORKCELL CONTROL SOFTWARE?

AUTOMATED WORKCELL CONTROL SOFTWARE is a medical device that received FDA 510(k) clearance on 2001-08-01. The listed applicant is Lab-Interlink, Inc.. The 510(k) number is K010500.

When did AUTOMATED WORKCELL CONTROL SOFTWARE receive FDA 510(k) clearance?

AUTOMATED WORKCELL CONTROL SOFTWARE received FDA 510(k) clearance on 2001-08-01, under 510(k) number K010500.

Who is the listed applicant for AUTOMATED WORKCELL CONTROL SOFTWARE?

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

What is the FDA product code for AUTOMATED WORKCELL CONTROL SOFTWARE?

The FDA product code for AUTOMATED WORKCELL CONTROL SOFTWARE is JJE.

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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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