FIXED-SIZE UTERINE DILATOR
K-Number: K890377 · 1989-02-13
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Device Summary
Frequently Asked Questions
What is the FIXED-SIZE UTERINE DILATOR?
FIXED-SIZE UTERINE DILATOR is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is Kinetic Medical Products. The 510(k) number is K890377.
When did FIXED-SIZE UTERINE DILATOR receive FDA 510(k) clearance?
FIXED-SIZE UTERINE DILATOR received FDA 510(k) clearance on 1989-02-13, under 510(k) number K890377.
Who is the listed applicant for FIXED-SIZE UTERINE DILATOR?
The FDA 510(k) record lists Kinetic Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIXED-SIZE UTERINE DILATOR?
The FDA product code for FIXED-SIZE UTERINE DILATOR is HDQ.
Related Clinical Trials
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.
Other records listing Kinetic Medical Products 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.
Related Devices (Code: HDQ)
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.
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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