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FDA 510(k)

MINIFLOW DISPOSABLE PRESSURE TRANSDUCER 63-600F

K-Number: K885296 · 1989-01-25

ApplicantBaxter Healthcare Corp
Decision Date1989-01-25
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINIFLOW DISPOSABLE PRESSURE TRANSDUCER 63-600F is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1989-01-25 under 510(k) number K885296. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIFLOW DISPOSABLE PRESSURE TRANSDUCER 63-600F?

MINIFLOW DISPOSABLE PRESSURE TRANSDUCER 63-600F is a medical device that received FDA 510(k) clearance on 1989-01-25. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K885296.

When did MINIFLOW DISPOSABLE PRESSURE TRANSDUCER 63-600F receive FDA 510(k) clearance?

MINIFLOW DISPOSABLE PRESSURE TRANSDUCER 63-600F received FDA 510(k) clearance on 1989-01-25, under 510(k) number K885296.

Who is the listed applicant for MINIFLOW DISPOSABLE PRESSURE TRANSDUCER 63-600F?

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

What is the FDA product code for MINIFLOW DISPOSABLE PRESSURE TRANSDUCER 63-600F?

The FDA product code for MINIFLOW DISPOSABLE PRESSURE TRANSDUCER 63-600F is DRS.

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Related Devices (Code: DRS)

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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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