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FDA 510(k)

MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY

K-Number: K052702 · 2005-11-21

ApplicantMisonix, Inc.
Decision Date2005-11-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Misonix, Inc.. It received FDA 510(k) clearance on 2005-11-21 under 510(k) number K052702. 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 MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY?

MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY is a medical device that received FDA 510(k) clearance on 2005-11-21. The listed applicant is Misonix, Inc.. The 510(k) number is K052702.

When did MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY receive FDA 510(k) clearance?

MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY received FDA 510(k) clearance on 2005-11-21, under 510(k) number K052702.

Who is the listed applicant for MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY?

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

What is the FDA product code for MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY?

The FDA product code for MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY is GEI.

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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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