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FDA 510(k)

SPERM WASHING MEDIUM #9983 & MODIFIED #9984

K-Number: K874668 · 1988-03-31

ApplicantIrvine Scientific
Decision Date1988-03-31
Product CodeHDR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SPERM WASHING MEDIUM #9983 & MODIFIED #9984 is the device name listed in this FDA 510(k) record. The listed applicant is Irvine Scientific. It received FDA 510(k) clearance on 1988-03-31 under 510(k) number K874668. 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 #9983 & MODIFIED #9984?

SPERM WASHING MEDIUM #9983 & MODIFIED #9984 is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Irvine Scientific. The 510(k) number is K874668.

When did SPERM WASHING MEDIUM #9983 & MODIFIED #9984 receive FDA 510(k) clearance?

SPERM WASHING MEDIUM #9983 & MODIFIED #9984 received FDA 510(k) clearance on 1988-03-31, under 510(k) number K874668.

Who is the listed applicant for SPERM WASHING MEDIUM #9983 & MODIFIED #9984?

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 #9983 & MODIFIED #9984?

The FDA product code for SPERM WASHING MEDIUM #9983 & MODIFIED #9984 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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