FDA 510(k)

ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA

K-Number: K882680 · 1988-07-22

Decision Date1988-07-22

Product CodeFJI

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA 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 1988-07-22 under 510(k) number K882680. The device is classified under product code FJI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA?

ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA is a medical device that received FDA 510(k) clearance on 1988-07-22. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K882680.

When did ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA receive FDA 510(k) clearance?

ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA received FDA 510(k) clearance on 1988-07-22, under 510(k) number K882680.

Who is the listed applicant for ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA?

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 ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA?

The FDA product code for ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA is FJI.

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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.