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FDA 510(k)

MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS

K-Number: K930355 · 1993-06-08

ApplicantMicrosurge, Inc.
Decision Date1993-06-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Microsurge, Inc.. It received FDA 510(k) clearance on 1993-06-08 under 510(k) number K930355. 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 MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS?

MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS is a medical device that received FDA 510(k) clearance on 1993-06-08. The listed applicant is Microsurge, Inc.. The 510(k) number is K930355.

When did MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS receive FDA 510(k) clearance?

MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS received FDA 510(k) clearance on 1993-06-08, under 510(k) number K930355.

Who is the listed applicant for MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS?

The FDA 510(k) record lists Microsurge, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS?

The FDA product code for MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS is GEI.

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Other records listing Microsurge, Inc. as applicant

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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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