FDA 510(k)

CONTINUOUS FLUSH DEVICE

K-Number: K792141 · 1979-12-05

ApplicantPharmaseal Div., Baxter Healthcare Corp.

Decision Date1979-12-05

Product CodeKRA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CONTINUOUS FLUSH DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Pharmaseal Div., Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1979-12-05 under 510(k) number K792141. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTINUOUS FLUSH DEVICE?

CONTINUOUS FLUSH DEVICE is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Pharmaseal Div., Baxter Healthcare Corp.. The 510(k) number is K792141.

When did CONTINUOUS FLUSH DEVICE receive FDA 510(k) clearance?

CONTINUOUS FLUSH DEVICE received FDA 510(k) clearance on 1979-12-05, under 510(k) number K792141.

Who is the listed applicant for CONTINUOUS FLUSH DEVICE?

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

What is the FDA product code for CONTINUOUS FLUSH DEVICE?

The FDA product code for CONTINUOUS FLUSH DEVICE is KRA.

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Other records listing Pharmaseal Div., Baxter Healthcare Corp. as applicant

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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.