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)

YESONA PLASTER OF PARIS BANDAGE

K-Number: K831492 · 1983-06-30

ApplicantWatson Phillips Y Cia. Sucs., S.A. DE C.V.
Decision Date1983-06-30
Product CodeITG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

YESONA PLASTER OF PARIS BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Watson Phillips Y Cia. Sucs., S.A. DE C.V.. It received FDA 510(k) clearance on 1983-06-30 under 510(k) number K831492. The device is classified under product code ITG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YESONA PLASTER OF PARIS BANDAGE?

YESONA PLASTER OF PARIS BANDAGE is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is Watson Phillips Y Cia. Sucs., S.A. DE C.V.. The 510(k) number is K831492.

When did YESONA PLASTER OF PARIS BANDAGE receive FDA 510(k) clearance?

YESONA PLASTER OF PARIS BANDAGE received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831492.

Who is the listed applicant for YESONA PLASTER OF PARIS BANDAGE?

The FDA 510(k) record lists Watson Phillips Y Cia. Sucs., S.A. DE C.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YESONA PLASTER OF PARIS BANDAGE?

The FDA product code for YESONA PLASTER OF PARIS BANDAGE is ITG.

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: ITG)

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.

K873111CONFORMA(TM) PLASTER BANDAGESThe Kendal Co.K862115DEKNA BAND KITDeknatel, Inc.K842573T.P.G. CAST TAPEThe Poly Group, Inc.K840416HEXCELITEHexcel MedicalK833732NON WETTING UNDERCAST PADDINGAmerican Medical Disposable, Inc.K832992SOFFBAN ORTHOPEDIC PADDINGSmith & Nephew, 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.

↑