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FDA 510(k)

SPERMCHECK VASECTOMY

K-Number: K073039 · 2008-01-24

ApplicantPrinceton BioMeditech Corp.
Decision Date2008-01-24
Product CodePOV
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SPERMCHECK VASECTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Princeton BioMeditech Corp.. It received FDA 510(k) clearance on 2008-01-24 under 510(k) number K073039. The device is classified under product code POV. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPERMCHECK VASECTOMY?

SPERMCHECK VASECTOMY is a medical device that received FDA 510(k) clearance on 2008-01-24. The listed applicant is Princeton BioMeditech Corp.. The 510(k) number is K073039.

When did SPERMCHECK VASECTOMY receive FDA 510(k) clearance?

SPERMCHECK VASECTOMY received FDA 510(k) clearance on 2008-01-24, under 510(k) number K073039.

Who is the listed applicant for SPERMCHECK VASECTOMY?

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

What is the FDA product code for SPERMCHECK VASECTOMY?

The FDA product code for SPERMCHECK VASECTOMY is POV.

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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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