MEDI-CULT UNIVERSAL IVF-MEDIUM
K-Number: K991279 · 2000-07-20
Advertisement
Device Summary
Frequently Asked Questions
What is the MEDI-CULT UNIVERSAL IVF-MEDIUM?
MEDI-CULT UNIVERSAL IVF-MEDIUM is a medical device that received FDA 510(k) clearance on 2000-07-20. The listed applicant is Medicult A/S. The 510(k) number is K991279.
When did MEDI-CULT UNIVERSAL IVF-MEDIUM receive FDA 510(k) clearance?
MEDI-CULT UNIVERSAL IVF-MEDIUM received FDA 510(k) clearance on 2000-07-20, under 510(k) number K991279.
Who is the listed applicant for MEDI-CULT UNIVERSAL IVF-MEDIUM?
The FDA 510(k) record lists Medicult A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDI-CULT UNIVERSAL IVF-MEDIUM?
The FDA product code for MEDI-CULT UNIVERSAL IVF-MEDIUM is MQL.
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 Medicult A/S 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: MQL)
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.
Advertisement