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FDA 510(k)

SPERM WASHING MEDIUM #9932

K-Number: K872102 · 1987-07-16

ApplicantIrvine Scientific
Decision Date1987-07-16
Product CodeHDR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SPERM WASHING MEDIUM #9932 is the device name listed in this FDA 510(k) record. The listed applicant is Irvine Scientific. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K872102. 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 SPERM WASHING MEDIUM #9932?

SPERM WASHING MEDIUM #9932 is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Irvine Scientific. The 510(k) number is K872102.

When did SPERM WASHING MEDIUM #9932 receive FDA 510(k) clearance?

SPERM WASHING MEDIUM #9932 received FDA 510(k) clearance on 1987-07-16, under 510(k) number K872102.

Who is the listed applicant for SPERM WASHING MEDIUM #9932?

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

What is the FDA product code for SPERM WASHING MEDIUM #9932?

The FDA product code for SPERM WASHING MEDIUM #9932 is HDR.

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Other records listing Irvine Scientific 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.

K160006Vit Kit-Freeze Oocytes, Embryos and PN zygotes Vitrification Freeze Kit, Vit Kit-Thaw Oocytes, Embryos and PN zygotes Vitrification Thaw KitK914541SPERM MAINTENANCE MEDIUM WITH GLYCEROLK900316MODIFIED HAM'S F-10 MEDIUM AND MEDIUM-HEPESK894405HTF WITH ALBUMIN (CATALOG NO. 9994)K894432MODIFIED HAM'S F-10 W/ALBUMINK874668SPERM WASHING MEDIUM #9983 & MODIFIED #9984

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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

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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