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FDA 510(k)

MINITUB MULTI-PURPOSE CASSETTES

K-Number: K002961 · 2000-11-21

Decision Date2000-11-21
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MINITUB MULTI-PURPOSE CASSETTES 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 2000-11-21 under 510(k) number K002961. 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 MINITUB MULTI-PURPOSE CASSETTES?

MINITUB MULTI-PURPOSE CASSETTES is a medical device that received FDA 510(k) clearance on 2000-11-21. The listed applicant is Zander Medical Supplies, Inc.. The 510(k) number is K002961.

When did MINITUB MULTI-PURPOSE CASSETTES receive FDA 510(k) clearance?

MINITUB MULTI-PURPOSE CASSETTES received FDA 510(k) clearance on 2000-11-21, under 510(k) number K002961.

Who is the listed applicant for MINITUB MULTI-PURPOSE CASSETTES?

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 MINITUB MULTI-PURPOSE CASSETTES?

The FDA product code for MINITUB MULTI-PURPOSE CASSETTES 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

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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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