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FDA 510(k)

ANGIOSCOPE W/INTEGRATED IRRIGATING CHANNEL

K-Number: K881469 · 1988-09-12

ApplicantBaxter Healthcare Corp
Decision Date1988-09-12
Product CodeFER
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ANGIOSCOPE W/INTEGRATED IRRIGATING CHANNEL 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 1988-09-12 under 510(k) number K881469. The device is classified under product code FER. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOSCOPE W/INTEGRATED IRRIGATING CHANNEL?

ANGIOSCOPE W/INTEGRATED IRRIGATING CHANNEL is a medical device that received FDA 510(k) clearance on 1988-09-12. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K881469.

When did ANGIOSCOPE W/INTEGRATED IRRIGATING CHANNEL receive FDA 510(k) clearance?

ANGIOSCOPE W/INTEGRATED IRRIGATING CHANNEL received FDA 510(k) clearance on 1988-09-12, under 510(k) number K881469.

Who is the listed applicant for ANGIOSCOPE W/INTEGRATED IRRIGATING CHANNEL?

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 ANGIOSCOPE W/INTEGRATED IRRIGATING CHANNEL?

The FDA product code for ANGIOSCOPE W/INTEGRATED IRRIGATING CHANNEL is FER.

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Other records listing Baxter Healthcare Corp as applicant

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Related Devices (Code: FER)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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