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FDA 510(k)

SPERM-SELECT ADDITIONAL INDICATION

K-Number: K872849 · 1987-09-28

ApplicantPharmacia, Inc.
Decision Date1987-09-28
Product CodeHDR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SPERM-SELECT ADDITIONAL INDICATION is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1987-09-28 under 510(k) number K872849. 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-SELECT ADDITIONAL INDICATION?

SPERM-SELECT ADDITIONAL INDICATION is a medical device that received FDA 510(k) clearance on 1987-09-28. The listed applicant is Pharmacia, Inc.. The 510(k) number is K872849.

When did SPERM-SELECT ADDITIONAL INDICATION receive FDA 510(k) clearance?

SPERM-SELECT ADDITIONAL INDICATION received FDA 510(k) clearance on 1987-09-28, under 510(k) number K872849.

Who is the listed applicant for SPERM-SELECT ADDITIONAL INDICATION?

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

What is the FDA product code for SPERM-SELECT ADDITIONAL INDICATION?

The FDA product code for SPERM-SELECT ADDITIONAL INDICATION is HDR.

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Other records listing Pharmacia, Inc. 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.

K974350ALLERGAN IMMUNO CAP M4, M8, K70K972364UNICAP PHADIATOPK972068UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0K964152UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMHK962274UNICAP 100

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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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