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FDA 510(k)

ENHANCE HTF MEDIUM WITH HEPES

K-Number: K023655 · 2002-12-13

Decision Date2002-12-13
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENHANCE HTF MEDIUM WITH HEPES is the device name listed in this FDA 510(k) record. The listed applicant is Conception Technologies. It received FDA 510(k) clearance on 2002-12-13 under 510(k) number K023655. 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 ENHANCE HTF MEDIUM WITH HEPES?

ENHANCE HTF MEDIUM WITH HEPES is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Conception Technologies. The 510(k) number is K023655.

When did ENHANCE HTF MEDIUM WITH HEPES receive FDA 510(k) clearance?

ENHANCE HTF MEDIUM WITH HEPES received FDA 510(k) clearance on 2002-12-13, under 510(k) number K023655.

Who is the listed applicant for ENHANCE HTF MEDIUM WITH HEPES?

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 ENHANCE HTF MEDIUM WITH HEPES?

The FDA product code for ENHANCE HTF MEDIUM WITH HEPES 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

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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