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FDA 510(k)

PBN FALLOPIAN TUBE CATHETER SYSTEM

K-Number: K000620 · 2000-10-30

ApplicantMedical Device Technologies, Inc.
Decision Date2000-10-30
Product CodeMDG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PBN FALLOPIAN TUBE CATHETER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 2000-10-30 under 510(k) number K000620. The device is classified under product code MDG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PBN FALLOPIAN TUBE CATHETER SYSTEM?

PBN FALLOPIAN TUBE CATHETER SYSTEM is a medical device that received FDA 510(k) clearance on 2000-10-30. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K000620.

When did PBN FALLOPIAN TUBE CATHETER SYSTEM receive FDA 510(k) clearance?

PBN FALLOPIAN TUBE CATHETER SYSTEM received FDA 510(k) clearance on 2000-10-30, under 510(k) number K000620.

Who is the listed applicant for PBN FALLOPIAN TUBE CATHETER SYSTEM?

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

What is the FDA product code for PBN FALLOPIAN TUBE CATHETER SYSTEM?

The FDA product code for PBN FALLOPIAN TUBE CATHETER SYSTEM is MDG.

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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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