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FDA 510(k)

INTRAUTERINE INSEMINATION CATHETERS

K-Number: K896960 · 1990-06-26

ApplicantC.R. Bard, Inc.
Decision Date1990-06-26
Product CodeHDR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INTRAUTERINE INSEMINATION CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1990-06-26 under 510(k) number K896960. The device is classified under product code HDR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAUTERINE INSEMINATION CATHETERS?

INTRAUTERINE INSEMINATION CATHETERS is a medical device that received FDA 510(k) clearance on 1990-06-26. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K896960.

When did INTRAUTERINE INSEMINATION CATHETERS receive FDA 510(k) clearance?

INTRAUTERINE INSEMINATION CATHETERS received FDA 510(k) clearance on 1990-06-26, under 510(k) number K896960.

Who is the listed applicant for INTRAUTERINE INSEMINATION CATHETERS?

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

What is the FDA product code for INTRAUTERINE INSEMINATION CATHETERS?

The FDA product code for INTRAUTERINE INSEMINATION CATHETERS is HDR.

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Related Devices (Code: HDR)

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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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