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FDA 510(k)

PILLING E-FRAZIER BIPOLAR SUCTION TUBE

K-Number: K002582 · 2000-11-03

ApplicantPilling
Decision Date2000-11-03
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PILLING E-FRAZIER BIPOLAR SUCTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Pilling. It received FDA 510(k) clearance on 2000-11-03 under 510(k) number K002582. 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 PILLING E-FRAZIER BIPOLAR SUCTION TUBE?

PILLING E-FRAZIER BIPOLAR SUCTION TUBE is a medical device that received FDA 510(k) clearance on 2000-11-03. The listed applicant is Pilling. The 510(k) number is K002582.

When did PILLING E-FRAZIER BIPOLAR SUCTION TUBE receive FDA 510(k) clearance?

PILLING E-FRAZIER BIPOLAR SUCTION TUBE received FDA 510(k) clearance on 2000-11-03, under 510(k) number K002582.

Who is the listed applicant for PILLING E-FRAZIER BIPOLAR SUCTION TUBE?

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

What is the FDA product code for PILLING E-FRAZIER BIPOLAR SUCTION TUBE?

The FDA product code for PILLING E-FRAZIER BIPOLAR SUCTION TUBE is GEI.

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Official Source

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