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FDA 510(k)

MONI-TROL-L AND MONI-TROL-XL

K-Number: K920291 · 1992-09-02

ApplicantMedical Analysis Systems, Inc.
Decision Date1992-09-02
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MONI-TROL-L AND MONI-TROL-XL 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 1992-09-02 under 510(k) number K920291. 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-L AND MONI-TROL-XL?

MONI-TROL-L AND MONI-TROL-XL is a medical device that received FDA 510(k) clearance on 1992-09-02. The listed applicant is Medical Analysis Systems, Inc.. The 510(k) number is K920291.

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

MONI-TROL-L AND MONI-TROL-XL received FDA 510(k) clearance on 1992-09-02, under 510(k) number K920291.

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

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-L AND MONI-TROL-XL?

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

Other records listing Medical Analysis Systems, Inc. as applicant

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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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