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FDA 510(k)

MEDI-CULT UNIVERSAL IVF-MEDIUM

K-Number: K991279 · 2000-07-20

ApplicantMedicult A/S
Decision Date2000-07-20
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDI-CULT UNIVERSAL IVF-MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Medicult A/S. It received FDA 510(k) clearance on 2000-07-20 under 510(k) number K991279. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 26 devices →

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.

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