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)

MILLONIG'S MODIFIED PHOSPHATE BUFFERED

K-Number: K830582 · 1983-03-17

ApplicantSurgipath Medical Industries, Inc.
Decision Date1983-03-17
Product CodeIFP
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

MILLONIG'S MODIFIED PHOSPHATE BUFFERED is the device name listed in this FDA 510(k) record. The listed applicant is Surgipath Medical Industries, Inc.. It received FDA 510(k) clearance on 1983-03-17 under 510(k) number K830582. The device is classified under product code IFP. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLONIG'S MODIFIED PHOSPHATE BUFFERED?

MILLONIG'S MODIFIED PHOSPHATE BUFFERED is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K830582.

When did MILLONIG'S MODIFIED PHOSPHATE BUFFERED receive FDA 510(k) clearance?

MILLONIG'S MODIFIED PHOSPHATE BUFFERED received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830582.

Who is the listed applicant for MILLONIG'S MODIFIED PHOSPHATE BUFFERED?

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

What is the FDA product code for MILLONIG'S MODIFIED PHOSPHATE BUFFERED?

The FDA product code for MILLONIG'S MODIFIED PHOSPHATE BUFFERED is IFP.

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 Surgipath Medical Industries, 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.

K883217SCHIFF REAGENTK881921C-E BRUSHK881922CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVEK881659TISSUE SECTION ADHESIVEK863549REUSABLE/DISPOSABLE AUTOPSY KNIFE SETK863616KNIFE MAKER

View all 30 devices →

Related Devices (Code: IFP)

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.

K884755CONSED FECAL CONCENTRATION SYSTEMDonald L. Price, Ph.D.K872663DRY-FORMAnatech, Ltd.K872140(MSI) PATH-SAVERMedical Specialties, Inc.K870852NBF 10% NEUTRAL BUFFERED FORMALINAnatech, Ltd.K853497PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALINSurgipath Medical Industries, Inc.K842982FORMALIN BUFFEREDReagent Laboratory, 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.

↑