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FDA 510(k)

INQU PASTE MIX

K-Number: K111838 · 2011-09-26

ApplicantIsto Technologies, Inc.
Decision Date2011-09-26
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INQU PASTE MIX is the device name listed in this FDA 510(k) record. The listed applicant is Isto Technologies, Inc.. It received FDA 510(k) clearance on 2011-09-26 under 510(k) number K111838. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INQU PASTE MIX?

INQU PASTE MIX is a medical device that received FDA 510(k) clearance on 2011-09-26. The listed applicant is Isto Technologies, Inc.. The 510(k) number is K111838.

When did INQU PASTE MIX receive FDA 510(k) clearance?

INQU PASTE MIX received FDA 510(k) clearance on 2011-09-26, under 510(k) number K111838.

Who is the listed applicant for INQU PASTE MIX?

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

What is the FDA product code for INQU PASTE MIX?

The FDA product code for INQU PASTE MIX is MQV.

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.

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Other records listing Isto Technologies, 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.

K103799INQU PASTE MIX PLUSK071428INQUK063359INQU

Related Devices (Code: MQV)

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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