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FDA 510(k)

IPT CAPSULE MIXER

K-Number: K922203 · 1992-06-03

ApplicantIpt Technologies, Inc.
Decision Date1992-06-03
Product CodeEFD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IPT CAPSULE MIXER is the device name listed in this FDA 510(k) record. The listed applicant is Ipt Technologies, Inc.. It received FDA 510(k) clearance on 1992-06-03 under 510(k) number K922203. The device is classified under product code EFD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPT CAPSULE MIXER?

IPT CAPSULE MIXER is a medical device that received FDA 510(k) clearance on 1992-06-03. The listed applicant is Ipt Technologies, Inc.. The 510(k) number is K922203.

When did IPT CAPSULE MIXER receive FDA 510(k) clearance?

IPT CAPSULE MIXER received FDA 510(k) clearance on 1992-06-03, under 510(k) number K922203.

Who is the listed applicant for IPT CAPSULE MIXER?

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

What is the FDA product code for IPT CAPSULE MIXER?

The FDA product code for IPT CAPSULE MIXER is EFD.

Related Clinical Trials

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Related Devices (Code: EFD)

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.

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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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