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FDA 510(k)

MINISPACE(TM) IUI CATHETER

K-Number: K902171 · 1990-10-05

ApplicantPharmacia, Inc.
Decision Date1990-10-05
Product CodeHDR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MINISPACE(TM) IUI CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1990-10-05 under 510(k) number K902171. 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 MINISPACE(TM) IUI CATHETER?

MINISPACE(TM) IUI CATHETER is a medical device that received FDA 510(k) clearance on 1990-10-05. The listed applicant is Pharmacia, Inc.. The 510(k) number is K902171.

When did MINISPACE(TM) IUI CATHETER receive FDA 510(k) clearance?

MINISPACE(TM) IUI CATHETER received FDA 510(k) clearance on 1990-10-05, under 510(k) number K902171.

Who is the listed applicant for MINISPACE(TM) IUI CATHETER?

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 MINISPACE(TM) IUI CATHETER?

The FDA product code for MINISPACE(TM) IUI CATHETER 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.K902694COAXIAL CATHETER SETCook Ob/Gyn

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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