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)

CIDEX ACTIVATED DIALDEHYDE SOLUTION

K-Number: K060618 · 2006-04-12

ApplicantJohnson & Johnson Co.
Decision Date2006-04-12
Product CodeMED
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CIDEX ACTIVATED DIALDEHYDE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Co.. It received FDA 510(k) clearance on 2006-04-12 under 510(k) number K060618. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIDEX ACTIVATED DIALDEHYDE SOLUTION?

CIDEX ACTIVATED DIALDEHYDE SOLUTION is a medical device that received FDA 510(k) clearance on 2006-04-12. The listed applicant is Johnson & Johnson Co.. The 510(k) number is K060618.

When did CIDEX ACTIVATED DIALDEHYDE SOLUTION receive FDA 510(k) clearance?

CIDEX ACTIVATED DIALDEHYDE SOLUTION received FDA 510(k) clearance on 2006-04-12, under 510(k) number K060618.

Who is the listed applicant for CIDEX ACTIVATED DIALDEHYDE SOLUTION?

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

What is the FDA product code for CIDEX ACTIVATED DIALDEHYDE SOLUTION?

The FDA product code for CIDEX ACTIVATED DIALDEHYDE SOLUTION is MED.

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: MED)

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.

K251666SYSTEM 1E Liquid Chemical Sterilant Processing System, Model P6700; SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900STERIS CorporationK232914SYSTEM 1E Liquid Chemical Sterilant Processing System (P6500); SYSTEM 1 endo Liquid Chemical Sterilant Processing System (P6800); SYSTEM 1 endo Liquid Chemical Sterilant Processing System (P6900)STERIS CorporationK230582SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900STERIS CorporationK222615SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6800, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900, S40 Sterilant ConcentrateSTERIS CorporationK211607SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6800, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900, S40 Sterilant ConcentrateSTERIS CorporationK210737SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6800, SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900, S40 Sterilant ConcentrateSTERIS Corporation

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.

↑