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FDA 510(k)

CAPIOX LEVEL ALARM

K-Number: K915337 · 1992-02-21

ApplicantTerumo Medical Corp.
Decision Date1992-02-21
Product CodeDTW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CAPIOX LEVEL ALARM is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1992-02-21 under 510(k) number K915337. The device is classified under product code DTW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPIOX LEVEL ALARM?

CAPIOX LEVEL ALARM is a medical device that received FDA 510(k) clearance on 1992-02-21. The listed applicant is Terumo Medical Corp.. The 510(k) number is K915337.

When did CAPIOX LEVEL ALARM receive FDA 510(k) clearance?

CAPIOX LEVEL ALARM received FDA 510(k) clearance on 1992-02-21, under 510(k) number K915337.

Who is the listed applicant for CAPIOX LEVEL ALARM?

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

What is the FDA product code for CAPIOX LEVEL ALARM?

The FDA product code for CAPIOX LEVEL ALARM is DTW.

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Other records listing Terumo Medical Corp. as applicant

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Related Devices (Code: DTW)

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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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