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FDA 510(k)

CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830

K-Number: K073022 · 2008-10-01

ApplicantClareblend, Inc.
Decision Date2008-10-01
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830 is the device name listed in this FDA 510(k) record. The listed applicant is Clareblend, Inc.. It received FDA 510(k) clearance on 2008-10-01 under 510(k) number K073022. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830?

CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830 is a medical device that received FDA 510(k) clearance on 2008-10-01. The listed applicant is Clareblend, Inc.. The 510(k) number is K073022.

When did CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830 receive FDA 510(k) clearance?

CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830 received FDA 510(k) clearance on 2008-10-01, under 510(k) number K073022.

Who is the listed applicant for CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830?

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

What is the FDA product code for CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830?

The FDA product code for CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830 is GEX. This falls under the Gastroenterology category.

Related Clinical Trials

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Other records listing Clareblend, 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.

K073000LUMAPROBEK880553ELECTRONIC EPILATOR

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Official Source

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