FDA 510(k)

QLICKSMART

K-Number: K983367 · 1998-11-06

Decision Date1998-11-06

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

QLICKSMART is the device name listed in this FDA 510(k) record. The listed applicant is Handren Assoc.. It received FDA 510(k) clearance on 1998-11-06 under 510(k) number K983367. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QLICKSMART?

QLICKSMART is a medical device that received FDA 510(k) clearance on 1998-11-06. The listed applicant is Handren Assoc.. The 510(k) number is K983367.

When did QLICKSMART receive FDA 510(k) clearance?

QLICKSMART received FDA 510(k) clearance on 1998-11-06, under 510(k) number K983367.

Who is the listed applicant for QLICKSMART?

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

What is the FDA product code for QLICKSMART?

The FDA product code for QLICKSMART is MMK.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: MMK)

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.