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FDA 510(k)

MAS LIQUID URINALYSIS CONTROL

K-Number: K935062 · 1994-01-27

Decision Date1994-01-27
Product CodeJJW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAS LIQUID URINALYSIS CONTROL 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 1994-01-27 under 510(k) number K935062. The device is classified under product code JJW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAS LIQUID URINALYSIS CONTROL?

MAS LIQUID URINALYSIS CONTROL is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Medical Analysis Systems, Inc.. The 510(k) number is K935062.

When did MAS LIQUID URINALYSIS CONTROL receive FDA 510(k) clearance?

MAS LIQUID URINALYSIS CONTROL received FDA 510(k) clearance on 1994-01-27, under 510(k) number K935062.

Who is the listed applicant for MAS LIQUID URINALYSIS CONTROL?

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 MAS LIQUID URINALYSIS CONTROL?

The FDA product code for MAS LIQUID URINALYSIS CONTROL is JJW.

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: JJW)

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

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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