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FDA 510(k)

ELECTROPROBE SINGLE-USE SURGICAL PROBE

K-Number: K903812 · 1990-09-20

ApplicantXimed Medical Systems
Decision Date1990-09-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROPROBE SINGLE-USE SURGICAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Ximed Medical Systems. It received FDA 510(k) clearance on 1990-09-20 under 510(k) number K903812. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROPROBE SINGLE-USE SURGICAL PROBE?

ELECTROPROBE SINGLE-USE SURGICAL PROBE is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is Ximed Medical Systems. The 510(k) number is K903812.

When did ELECTROPROBE SINGLE-USE SURGICAL PROBE receive FDA 510(k) clearance?

ELECTROPROBE SINGLE-USE SURGICAL PROBE received FDA 510(k) clearance on 1990-09-20, under 510(k) number K903812.

Who is the listed applicant for ELECTROPROBE SINGLE-USE SURGICAL PROBE?

The FDA 510(k) record lists Ximed Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROPROBE SINGLE-USE SURGICAL PROBE?

The FDA product code for ELECTROPROBE SINGLE-USE SURGICAL PROBE is GEI.

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Other records listing Ximed Medical Systems as applicant

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.

K943014BALLOON ELECTROSURGICAL PROBES AND DEVICESK946377ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBESK933757HAND-HELD IRRIGATION PUMPK933458SURGICAL TROCARSK922714UNIVERSAL IRRIGATION & SUCTION TUBING SETK922523BIPOLAR ELECTROSURGICAL PROBES & INSTRUMENTS

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Related Devices (Code: GEI)

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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