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FDA 510(k)

MTG - MINITUB HEATED STAGE SYSTEMS

K-Number: K002971 · 2000-12-15

Decision Date2000-12-15
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MTG - MINITUB HEATED STAGE SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Zander Medical Supplies, Inc.. It received FDA 510(k) clearance on 2000-12-15 under 510(k) number K002971. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTG - MINITUB HEATED STAGE SYSTEMS?

MTG - MINITUB HEATED STAGE SYSTEMS is a medical device that received FDA 510(k) clearance on 2000-12-15. The listed applicant is Zander Medical Supplies, Inc.. The 510(k) number is K002971.

When did MTG - MINITUB HEATED STAGE SYSTEMS receive FDA 510(k) clearance?

MTG - MINITUB HEATED STAGE SYSTEMS received FDA 510(k) clearance on 2000-12-15, under 510(k) number K002971.

Who is the listed applicant for MTG - MINITUB HEATED STAGE SYSTEMS?

The FDA 510(k) record lists Zander Medical Supplies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MTG - MINITUB HEATED STAGE SYSTEMS?

The FDA product code for MTG - MINITUB HEATED STAGE SYSTEMS is MQG.

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 Zander Medical Supplies, Inc. 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.

Related Devices (Code: MQG)

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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