Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DEFOGGING AND CLEANING SOLUTION- FLO-X

K-Number: K102452 · 2010-12-23

Decision Date2010-12-23
Product CodeOCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DEFOGGING AND CLEANING SOLUTION- FLO-X is the device name listed in this FDA 510(k) record. The listed applicant is Minimally Invasive Devices, LLC. It received FDA 510(k) clearance on 2010-12-23 under 510(k) number K102452. The device is classified under product code OCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEFOGGING AND CLEANING SOLUTION- FLO-X?

DEFOGGING AND CLEANING SOLUTION- FLO-X is a medical device that received FDA 510(k) clearance on 2010-12-23. The listed applicant is Minimally Invasive Devices, LLC. The 510(k) number is K102452.

When did DEFOGGING AND CLEANING SOLUTION- FLO-X receive FDA 510(k) clearance?

DEFOGGING AND CLEANING SOLUTION- FLO-X received FDA 510(k) clearance on 2010-12-23, under 510(k) number K102452.

Who is the listed applicant for DEFOGGING AND CLEANING SOLUTION- FLO-X?

The FDA 510(k) record lists Minimally Invasive Devices, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEFOGGING AND CLEANING SOLUTION- FLO-X?

The FDA product code for DEFOGGING AND CLEANING SOLUTION- FLO-X is OCT.

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 Minimally Invasive Devices, LLC 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: OCT)

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.

↑