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FDA 510(k)

FLUOROSTAT FLUOROMETER

K-Number: K822701 · 1982-10-08

Decision Date1982-10-08
Product CodeKHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FLUOROSTAT FLUOROMETER 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 1982-10-08 under 510(k) number K822701. The device is classified under product code KHO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUOROSTAT FLUOROMETER?

FLUOROSTAT FLUOROMETER is a medical device that received FDA 510(k) clearance on 1982-10-08. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K822701.

When did FLUOROSTAT FLUOROMETER receive FDA 510(k) clearance?

FLUOROSTAT FLUOROMETER received FDA 510(k) clearance on 1982-10-08, under 510(k) number K822701.

Who is the listed applicant for FLUOROSTAT FLUOROMETER?

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 FLUOROSTAT FLUOROMETER?

The FDA product code for FLUOROSTAT FLUOROMETER is KHO.

Related Clinical Trials

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.

Other records listing Miles Laboratories, Inc. as applicant

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.

View all 158 devices →

Related Devices (Code: KHO)

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.

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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