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)

100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2

K-Number: K861890 · 1986-06-03

ApplicantRichard-Allan Medical Ind., Inc.
Decision Date1986-06-03
Product CodePPM
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2 is the device name listed in this FDA 510(k) record. The listed applicant is Richard-Allan Medical Ind., Inc.. It received FDA 510(k) clearance on 1986-06-03 under 510(k) number K861890. The device is classified under product code PPM. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2?

100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2 is a medical device that received FDA 510(k) clearance on 1986-06-03. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K861890.

When did 100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2 receive FDA 510(k) clearance?

100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2 received FDA 510(k) clearance on 1986-06-03, under 510(k) number K861890.

Who is the listed applicant for 100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2?

The FDA 510(k) record lists Richard-Allan Medical Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2?

The FDA product code for 100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2 is PPM.

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

Other records listing Richard-Allan Medical Ind., 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.

K931879REFLEX HTRK924200REFLEX(R) ESCK926297REFLEX ESIK924761STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELDK900566RICHARD-ALLAN VESSEL LOOPSK896262TITANIUM LIGATING CLIPS

View all 33 devices →

Related Devices (Code: PPM)

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.

K871533TOMTEC GRAM STAINER DECOLORIZERRemel Co.K863550POTASSIUM HYDROXIDE 10% W/VReagent Laboratory, Inc.K850916SPRAYFIXSurgipath Medical Industries, Inc.K8508450.85% SALINEMicro Media LaboratoriesK850737TRANSPORT CULTURE MEDIUMRoseville Medical LaboratoriesuK842934DECOLORIZING FLUIC, ACID-ALCOHOL 3%E K Ind., Inc.

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.

↑