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FDA 510(k)

MASTER ALERT

K-Number: K934848 · 1994-09-29

ApplicantMaster Hydro Systems, Inc.
Decision Date1994-09-29
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MASTER ALERT is the device name listed in this FDA 510(k) record. The listed applicant is Master Hydro Systems, Inc.. It received FDA 510(k) clearance on 1994-09-29 under 510(k) number K934848. The device is classified under product code FIP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTER ALERT?

MASTER ALERT is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Master Hydro Systems, Inc.. The 510(k) number is K934848.

When did MASTER ALERT receive FDA 510(k) clearance?

MASTER ALERT received FDA 510(k) clearance on 1994-09-29, under 510(k) number K934848.

Who is the listed applicant for MASTER ALERT?

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

What is the FDA product code for MASTER ALERT?

The FDA product code for MASTER ALERT is FIP.

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Related Devices (Code: FIP)

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

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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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