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FDA 510(k)

FERTILOSCOPY KIT FH 1.29/FTO 1.40

K-Number: K992655 · 2000-03-13

ApplicantSoprane S.A.
Decision Date2000-03-13
Product CodeHEW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FERTILOSCOPY KIT FH 1.29/FTO 1.40 is the device name listed in this FDA 510(k) record. The listed applicant is Soprane S.A.. It received FDA 510(k) clearance on 2000-03-13 under 510(k) number K992655. The device is classified under product code HEW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FERTILOSCOPY KIT FH 1.29/FTO 1.40?

FERTILOSCOPY KIT FH 1.29/FTO 1.40 is a medical device that received FDA 510(k) clearance on 2000-03-13. The listed applicant is Soprane S.A.. The 510(k) number is K992655.

When did FERTILOSCOPY KIT FH 1.29/FTO 1.40 receive FDA 510(k) clearance?

FERTILOSCOPY KIT FH 1.29/FTO 1.40 received FDA 510(k) clearance on 2000-03-13, under 510(k) number K992655.

Who is the listed applicant for FERTILOSCOPY KIT FH 1.29/FTO 1.40?

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

What is the FDA product code for FERTILOSCOPY KIT FH 1.29/FTO 1.40?

The FDA product code for FERTILOSCOPY KIT FH 1.29/FTO 1.40 is HEW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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