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FDA 510(k)

INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS

K-Number: K904173 · 1990-12-10

ApplicantBaxter Healthcare Corp
Decision Date1990-12-10
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS 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 1990-12-10 under 510(k) number K904173. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS?

INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS is a medical device that received FDA 510(k) clearance on 1990-12-10. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K904173.

When did INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS receive FDA 510(k) clearance?

INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS received FDA 510(k) clearance on 1990-12-10, under 510(k) number K904173.

Who is the listed applicant for INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS?

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 INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS?

The FDA product code for INSULATED ELECTRODES AND LAPAROSCOPIC PROBICS is HET.

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Related Devices (Code: HET)

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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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