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FDA 510(k)

RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET

K-Number: K884696 · 1989-01-27

ApplicantLaboratoire Ccd C/O Washington Regulatory Services
Decision Date1989-01-27
Product CodeHDR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Laboratoire Ccd C/O Washington Regulatory Services. It received FDA 510(k) clearance on 1989-01-27 under 510(k) number K884696. 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 RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET?

RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET is a medical device that received FDA 510(k) clearance on 1989-01-27. The listed applicant is Laboratoire Ccd C/O Washington Regulatory Services. The 510(k) number is K884696.

When did RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET receive FDA 510(k) clearance?

RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET received FDA 510(k) clearance on 1989-01-27, under 510(k) number K884696.

Who is the listed applicant for RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET?

The FDA 510(k) record lists Laboratoire Ccd C/O Washington Regulatory Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET?

The FDA product code for RESUBMITTED ARTIFICIAL INSEMINATION INSTRUMENT SET is HDR.

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Other records listing Laboratoire Ccd C/O Washington Regulatory Services as applicant

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.

K890706CYTOBRUSHK881456PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTEK881220ENDOCYTE, DISPOSABLE ENDOMETRIAL SAMPLER

Related Devices (Code: HDR)

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.

K242031Béa Applicator (BAP-GB-01)Stepone Fertility Ltd (T/A Béa Fertility)K222969FERTI-LILY Conception CupRosesta Medical BVK993953OVES CERVICAL CAPVeos , Ltd.K945131IMAGYN INTRAUTERINE INSEMINATION DEVICEImagyn Medical, Inc.K950714COOK INSEMINATION CUPCook Urological, Inc.K902171MINISPACE(TM) IUI CATHETERPharmacia, Inc.

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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