FDA 510(k)

PHARMASEAL EPIDURAL CATHETER & CONTINUOUS EPIDURAL

K-Number: K897194 · 1990-06-18

Decision Date1990-06-18

Product CodeBSO

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PHARMASEAL EPIDURAL CATHETER & CONTINUOUS EPIDURAL 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 1990-06-18 under 510(k) number K897194. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARMASEAL EPIDURAL CATHETER & CONTINUOUS EPIDURAL?

PHARMASEAL EPIDURAL CATHETER & CONTINUOUS EPIDURAL is a medical device that received FDA 510(k) clearance on 1990-06-18. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K897194.

When did PHARMASEAL EPIDURAL CATHETER & CONTINUOUS EPIDURAL receive FDA 510(k) clearance?

PHARMASEAL EPIDURAL CATHETER & CONTINUOUS EPIDURAL received FDA 510(k) clearance on 1990-06-18, under 510(k) number K897194.

Who is the listed applicant for PHARMASEAL EPIDURAL CATHETER & CONTINUOUS EPIDURAL?

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 PHARMASEAL EPIDURAL CATHETER & CONTINUOUS EPIDURAL?

The FDA product code for PHARMASEAL EPIDURAL CATHETER & CONTINUOUS EPIDURAL is BSO.

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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.