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FDA 510(k)

MODEL 5030 SUCTION HANDPIECE SYSTEM

K-Number: K933017 · 1993-07-26

ApplicantSunrise Technologies, Inc.
Decision Date1993-07-26
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL 5030 SUCTION HANDPIECE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Technologies, Inc.. It received FDA 510(k) clearance on 1993-07-26 under 510(k) number K933017. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 5030 SUCTION HANDPIECE SYSTEM?

MODEL 5030 SUCTION HANDPIECE SYSTEM is a medical device that received FDA 510(k) clearance on 1993-07-26. The listed applicant is Sunrise Technologies, Inc.. The 510(k) number is K933017.

When did MODEL 5030 SUCTION HANDPIECE SYSTEM receive FDA 510(k) clearance?

MODEL 5030 SUCTION HANDPIECE SYSTEM received FDA 510(k) clearance on 1993-07-26, under 510(k) number K933017.

Who is the listed applicant for MODEL 5030 SUCTION HANDPIECE SYSTEM?

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

What is the FDA product code for MODEL 5030 SUCTION HANDPIECE SYSTEM?

The FDA product code for MODEL 5030 SUCTION HANDPIECE SYSTEM is GEX. This falls under the Gastroenterology category.

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Other records listing Sunrise Technologies, Inc. as applicant

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Related Devices (Code: GEX)

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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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