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FDA 510(k)

MONI-TROL XL AND L UNASSAYED LIQUID CHEMISTRY

K-Number: K903190 · 1990-08-17

Decision Date1990-08-17
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MONI-TROL XL AND L UNASSAYED LIQUID CHEMISTRY is the device name listed in this FDA 510(k) record. The listed applicant is Medical Analysis Systems, Inc.. It received FDA 510(k) clearance on 1990-08-17 under 510(k) number K903190. 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 MONI-TROL XL AND L UNASSAYED LIQUID CHEMISTRY?

MONI-TROL XL AND L UNASSAYED LIQUID CHEMISTRY is a medical device that received FDA 510(k) clearance on 1990-08-17. The listed applicant is Medical Analysis Systems, Inc.. The 510(k) number is K903190.

When did MONI-TROL XL AND L UNASSAYED LIQUID CHEMISTRY receive FDA 510(k) clearance?

MONI-TROL XL AND L UNASSAYED LIQUID CHEMISTRY received FDA 510(k) clearance on 1990-08-17, under 510(k) number K903190.

Who is the listed applicant for MONI-TROL XL AND L UNASSAYED LIQUID CHEMISTRY?

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

What is the FDA product code for MONI-TROL XL AND L UNASSAYED LIQUID CHEMISTRY?

The FDA product code for MONI-TROL XL AND L UNASSAYED LIQUID CHEMISTRY is JJY.

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 Medical Analysis Systems, 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 107 devices →

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.

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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