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FDA 510(k)

NUNC IVF DISHES AND NUNC IVF 4-WELL DISH

K-Number: K070047 · 2007-05-18

ApplicantNunc A/S
Decision Date2007-05-18
Product CodeMQK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NUNC IVF DISHES AND NUNC IVF 4-WELL DISH is the device name listed in this FDA 510(k) record. The listed applicant is Nunc A/S. It received FDA 510(k) clearance on 2007-05-18 under 510(k) number K070047. The device is classified under product code MQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUNC IVF DISHES AND NUNC IVF 4-WELL DISH?

NUNC IVF DISHES AND NUNC IVF 4-WELL DISH is a medical device that received FDA 510(k) clearance on 2007-05-18. The listed applicant is Nunc A/S. The 510(k) number is K070047.

When did NUNC IVF DISHES AND NUNC IVF 4-WELL DISH receive FDA 510(k) clearance?

NUNC IVF DISHES AND NUNC IVF 4-WELL DISH received FDA 510(k) clearance on 2007-05-18, under 510(k) number K070047.

Who is the listed applicant for NUNC IVF DISHES AND NUNC IVF 4-WELL DISH?

The FDA 510(k) record lists Nunc A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NUNC IVF DISHES AND NUNC IVF 4-WELL DISH?

The FDA product code for NUNC IVF DISHES AND NUNC IVF 4-WELL DISH is MQK.

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Other records listing Nunc 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.

K040717NUNC IVF MULTIDISH 4 WELLS NUNCLON

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Official Source

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