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FDA 510(k)

CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL

K-Number: K932387 · 1995-03-06

ApplicantConceptus, Inc.
Decision Date1995-03-06
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL is the device name listed in this FDA 510(k) record. The listed applicant is Conceptus, Inc.. It received FDA 510(k) clearance on 1995-03-06 under 510(k) number K932387. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL?

CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL is a medical device that received FDA 510(k) clearance on 1995-03-06. The listed applicant is Conceptus, Inc.. The 510(k) number is K932387.

When did CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL receive FDA 510(k) clearance?

CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL received FDA 510(k) clearance on 1995-03-06, under 510(k) number K932387.

Who is the listed applicant for CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL?

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

What is the FDA product code for CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL?

The FDA product code for CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL is HET.

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Other records listing Conceptus, Inc. as applicant

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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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