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FDA 510(k)

CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM

K-Number: K932722 · 1993-08-06

ApplicantCarie Med-Tech Services, Inc.
Decision Date1993-08-06
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Carie Med-Tech Services, Inc.. It received FDA 510(k) clearance on 1993-08-06 under 510(k) number K932722. 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 CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM?

CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is Carie Med-Tech Services, Inc.. The 510(k) number is K932722.

When did CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM receive FDA 510(k) clearance?

CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM received FDA 510(k) clearance on 1993-08-06, under 510(k) number K932722.

Who is the listed applicant for CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM?

The FDA 510(k) record lists Carie Med-Tech Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM?

The FDA product code for CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEM is BYH.

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Related Devices (Code: BYH)

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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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