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FDA 510(k)

KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL

K-Number: K903338 · 1990-09-07

ApplicantKenlor Industries, Inc.
Decision Date1990-09-07
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Kenlor Industries, Inc.. It received FDA 510(k) clearance on 1990-09-07 under 510(k) number K903338. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL?

KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL is a medical device that received FDA 510(k) clearance on 1990-09-07. The listed applicant is Kenlor Industries, Inc.. The 510(k) number is K903338.

When did KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL receive FDA 510(k) clearance?

KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL received FDA 510(k) clearance on 1990-09-07, under 510(k) number K903338.

Who is the listed applicant for KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL?

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

What is the FDA product code for KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL?

The FDA product code for KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROL is JJY.

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Other records listing Kenlor Industries, Inc. as applicant

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Related Devices (Code: JJY)

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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