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FDA 510(k)

THE BIO-TEK CHROMOSCAN

K-Number: K803030 · 1980-12-22

ApplicantBio-Tek Instruments, Inc.
Decision Date1980-12-22
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

THE BIO-TEK CHROMOSCAN 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 1980-12-22 under 510(k) number K803030. 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 THE BIO-TEK CHROMOSCAN?

THE BIO-TEK CHROMOSCAN is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Bio-Tek Instruments, Inc.. The 510(k) number is K803030.

When did THE BIO-TEK CHROMOSCAN receive FDA 510(k) clearance?

THE BIO-TEK CHROMOSCAN received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803030.

Who is the listed applicant for THE BIO-TEK CHROMOSCAN?

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

What is the FDA product code for THE BIO-TEK CHROMOSCAN?

The FDA product code for THE BIO-TEK CHROMOSCAN is JJQ.

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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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