INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL
K-Number: K092840 · 2009-12-03
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Device Summary
Frequently Asked Questions
What is the INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL?
INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL is a medical device that received FDA 510(k) clearance on 2009-12-03. The listed applicant is Instrumed International, Inc.. The 510(k) number is K092840.
When did INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL receive FDA 510(k) clearance?
INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL received FDA 510(k) clearance on 2009-12-03, under 510(k) number K092840.
Who is the listed applicant for INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL?
The FDA 510(k) record lists Instrumed International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL?
The FDA product code for INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL is HCZ.
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 Instrumed International, 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.
Related Devices (Code: HCZ)
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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