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FDA 510(k)

OIL FOR TISSUE CULTURE

K-Number: K011462 · 2001-06-13

Decision Date2001-06-13
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OIL FOR TISSUE CULTURE is the device name listed in this FDA 510(k) record. The listed applicant is Conception Technologies. It received FDA 510(k) clearance on 2001-06-13 under 510(k) number K011462. 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 OIL FOR TISSUE CULTURE?

OIL FOR TISSUE CULTURE is a medical device that received FDA 510(k) clearance on 2001-06-13. The listed applicant is Conception Technologies. The 510(k) number is K011462.

When did OIL FOR TISSUE CULTURE receive FDA 510(k) clearance?

OIL FOR TISSUE CULTURE received FDA 510(k) clearance on 2001-06-13, under 510(k) number K011462.

Who is the listed applicant for OIL FOR TISSUE CULTURE?

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

What is the FDA product code for OIL FOR TISSUE CULTURE?

The FDA product code for OIL FOR TISSUE CULTURE 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 Conception Technologies 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 8 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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