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FDA 510(k)

PBN HYSTERO-SALPINGOGRAPHY CATHETER SET

K-Number: K000433 · 2000-06-16

ApplicantMedical Device Technologies, Inc.
Decision Date2000-06-16
Product CodeLKF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PBN HYSTERO-SALPINGOGRAPHY CATHETER SET 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 2000-06-16 under 510(k) number K000433. The device is classified under product code LKF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PBN HYSTERO-SALPINGOGRAPHY CATHETER SET?

PBN HYSTERO-SALPINGOGRAPHY CATHETER SET is a medical device that received FDA 510(k) clearance on 2000-06-16. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K000433.

When did PBN HYSTERO-SALPINGOGRAPHY CATHETER SET receive FDA 510(k) clearance?

PBN HYSTERO-SALPINGOGRAPHY CATHETER SET received FDA 510(k) clearance on 2000-06-16, under 510(k) number K000433.

Who is the listed applicant for PBN HYSTERO-SALPINGOGRAPHY CATHETER SET?

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 HYSTERO-SALPINGOGRAPHY CATHETER SET?

The FDA product code for PBN HYSTERO-SALPINGOGRAPHY CATHETER SET is LKF.

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Related Devices (Code: LKF)

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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