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FDA 510(k)

MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000)

K-Number: K884782 · 1989-02-17

ApplicantDynatech Laboratories, Inc.
Decision Date1989-02-17
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000) is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Laboratories, Inc.. It received FDA 510(k) clearance on 1989-02-17 under 510(k) number K884782. 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 MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000)?

MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000) is a medical device that received FDA 510(k) clearance on 1989-02-17. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K884782.

When did MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000) receive FDA 510(k) clearance?

MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000) received FDA 510(k) clearance on 1989-02-17, under 510(k) number K884782.

Who is the listed applicant for MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000)?

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

What is the FDA product code for MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000)?

The FDA product code for MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000) is JJQ.

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Related Devices (Code: JJQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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