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)

PICIS WEIGHT BASED DOSE CONVERTER

K-Number: K121542 · 2012-08-27

ApplicantPicis, Inc.
Decision Date2012-08-27
Product CodeNDC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PICIS WEIGHT BASED DOSE CONVERTER is the device name listed in this FDA 510(k) record. The listed applicant is Picis, Inc.. It received FDA 510(k) clearance on 2012-08-27 under 510(k) number K121542. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PICIS WEIGHT BASED DOSE CONVERTER?

PICIS WEIGHT BASED DOSE CONVERTER is a medical device that received FDA 510(k) clearance on 2012-08-27. The listed applicant is Picis, Inc.. The 510(k) number is K121542.

When did PICIS WEIGHT BASED DOSE CONVERTER receive FDA 510(k) clearance?

PICIS WEIGHT BASED DOSE CONVERTER received FDA 510(k) clearance on 2012-08-27, under 510(k) number K121542.

Who is the listed applicant for PICIS WEIGHT BASED DOSE CONVERTER?

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

What is the FDA product code for PICIS WEIGHT BASED DOSE CONVERTER?

The FDA product code for PICIS WEIGHT BASED DOSE CONVERTER is NDC.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: NDC)

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.

K254102GlucommanderGlytec, LLCK260910EndoTool IV Cloud 1.0Glooko, Inc.K253512MiniMed Go AppMedtronic MinimedK253281UpDocUpdoc, Inc.K252104T1D1Comerge AGK241088EndoTool IV (3.1)Monarch Medical Technologies

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.

↑