FDA 510(k)

SAFETY DRAIN

K-Number: K881790 · 1988-06-21

Decision Date1988-06-21

Product CodeBYH

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

SAFETY DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is Ballard Medical Products. It received FDA 510(k) clearance on 1988-06-21 under 510(k) number K881790. The device is classified under product code BYH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFETY DRAIN?

SAFETY DRAIN is a medical device that received FDA 510(k) clearance on 1988-06-21. The listed applicant is Ballard Medical Products. The 510(k) number is K881790.

When did SAFETY DRAIN receive FDA 510(k) clearance?

SAFETY DRAIN received FDA 510(k) clearance on 1988-06-21, under 510(k) number K881790.

Who is the listed applicant for SAFETY DRAIN?

The FDA 510(k) record lists Ballard Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFETY DRAIN?

The FDA product code for SAFETY DRAIN is BYH.

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Other records listing Ballard Medical Products as applicant

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Related Devices (Code: BYH)

K946057AQUALARM MOISTURE SENSOR MODEL P85000Pegasus Research Corp.K932722CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEMCarie Med-Tech Services, Inc.K921624DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITSIntertech Resources, Inc.K900047THAYER SUCTION EVACUATION CONDENSATE COLLECTIONThayer Medical Corp.K897057THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEMThayer Medical Corp.K895479THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEMThayer Medical Corp.

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.