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FDA 510(k)

MV/CM2 NUMBER X74294 MODEL NUMBER 74229

K-Number: K837605 · 1983-06-28

ApplicantBio-Tek Instruments, Inc.
Decision Date1983-06-28
Product Code
DecisionSubstantially Equivalent

Device Summary

MV/CM2 NUMBER X74294 MODEL NUMBER 74229 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Tek Instruments, Inc.. It received FDA 510(k) clearance on 1983-06-28 under 510(k) number K837605. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MV/CM2 NUMBER X74294 MODEL NUMBER 74229?

MV/CM2 NUMBER X74294 MODEL NUMBER 74229 is a medical device that received FDA 510(k) clearance on 1983-06-28. The listed applicant is Bio-Tek Instruments, Inc.. The 510(k) number is K837605.

When did MV/CM2 NUMBER X74294 MODEL NUMBER 74229 receive FDA 510(k) clearance?

MV/CM2 NUMBER X74294 MODEL NUMBER 74229 received FDA 510(k) clearance on 1983-06-28, under 510(k) number K837605.

Who is the listed applicant for MV/CM2 NUMBER X74294 MODEL NUMBER 74229?

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

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Other records listing Bio-Tek Instruments, Inc. as applicant

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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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