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FDA 510(k)

CLINI-TEK AUTO 2000 REFLECTANCE SPECTR

K-Number: K841041 · 1984-08-24

ApplicantMiles Laboratories, Inc.
Decision Date1984-08-24
Product CodeKQO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CLINI-TEK AUTO 2000 REFLECTANCE SPECTR is the device name listed in this FDA 510(k) record. The listed applicant is Miles Laboratories, Inc.. It received FDA 510(k) clearance on 1984-08-24 under 510(k) number K841041. The device is classified under product code KQO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINI-TEK AUTO 2000 REFLECTANCE SPECTR?

CLINI-TEK AUTO 2000 REFLECTANCE SPECTR is a medical device that received FDA 510(k) clearance on 1984-08-24. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K841041.

When did CLINI-TEK AUTO 2000 REFLECTANCE SPECTR receive FDA 510(k) clearance?

CLINI-TEK AUTO 2000 REFLECTANCE SPECTR received FDA 510(k) clearance on 1984-08-24, under 510(k) number K841041.

Who is the listed applicant for CLINI-TEK AUTO 2000 REFLECTANCE SPECTR?

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

What is the FDA product code for CLINI-TEK AUTO 2000 REFLECTANCE SPECTR?

The FDA product code for CLINI-TEK AUTO 2000 REFLECTANCE SPECTR is KQO.

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Other records listing Miles Laboratories, Inc. as applicant

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Related Devices (Code: KQO)

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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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