FDA 510(k)

BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES

K-Number: K880637 · 1988-04-11

Decision Date1988-04-11

Product CodeBZO

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES 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 1988-04-11 under 510(k) number K880637. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES?

BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES is a medical device that received FDA 510(k) clearance on 1988-04-11. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K880637.

When did BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES receive FDA 510(k) clearance?

BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES received FDA 510(k) clearance on 1988-04-11, under 510(k) number K880637.

Who is the listed applicant for BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES?

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 BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES?

The FDA product code for BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES is BZO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.