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FDA 510(k)

REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA

K-Number: K894259 · 1990-03-05

ApplicantWashington Regulatory Services
Decision Date1990-03-05
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA is the device name listed in this FDA 510(k) record. The listed applicant is Washington Regulatory Services. It received FDA 510(k) clearance on 1990-03-05 under 510(k) number K894259. The device is classified under product code HIG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA?

REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA is a medical device that received FDA 510(k) clearance on 1990-03-05. The listed applicant is Washington Regulatory Services. The 510(k) number is K894259.

When did REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA receive FDA 510(k) clearance?

REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA received FDA 510(k) clearance on 1990-03-05, under 510(k) number K894259.

Who is the listed applicant for REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA?

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

What is the FDA product code for REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA?

The FDA product code for REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA is HIG.

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Other records listing 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.

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Related Devices (Code: HIG)

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.

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Official Source

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