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FDA 510(k)

NIDOIL

K-Number: K012123 · 2001-08-03

Decision Date2001-08-03
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NIDOIL is the device name listed in this FDA 510(k) record. The listed applicant is Nidacon International AB. It received FDA 510(k) clearance on 2001-08-03 under 510(k) number K012123. 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 NIDOIL?

NIDOIL is a medical device that received FDA 510(k) clearance on 2001-08-03. The listed applicant is Nidacon International AB. The 510(k) number is K012123.

When did NIDOIL receive FDA 510(k) clearance?

NIDOIL received FDA 510(k) clearance on 2001-08-03, under 510(k) number K012123.

Who is the listed applicant for NIDOIL?

The FDA 510(k) record lists Nidacon International AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIDOIL?

The FDA product code for NIDOIL 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 Nidacon International AB 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 11 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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