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)

KENDALL CURITY BURN PAD

K-Number: K853145 · 1985-08-30

ApplicantThe Kendal Co.
Decision Date1985-08-30
Product CodeFPY
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

KENDALL CURITY BURN PAD is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1985-08-30 under 510(k) number K853145. The device is classified under product code FPY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the KENDALL CURITY BURN PAD?

KENDALL CURITY BURN PAD is a medical device that received FDA 510(k) clearance on 1985-08-30. The listed applicant is The Kendal Co.. The 510(k) number is K853145.

When did KENDALL CURITY BURN PAD receive FDA 510(k) clearance?

KENDALL CURITY BURN PAD received FDA 510(k) clearance on 1985-08-30, under 510(k) number K853145.

Who is the listed applicant for KENDALL CURITY BURN PAD?

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

What is the FDA product code for KENDALL CURITY BURN PAD?

The FDA product code for KENDALL CURITY BURN PAD is FPY.

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 The Kendal Co. 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.

K000087MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FRK990500KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946CK991758MONOJECT INSULIN SYRINGEK970969KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SETK951488KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAPK942664KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM

View all 63 devices →

Related Devices (Code: FPY)

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.

K930759CP & S STERILE BURN SHEETConsolidated Products & Services, Inc.K921470BURNSHIELD FIRE BLANKETLevtrade Intl. (Pty) , Ltd.K921471BURNSHIELD TRAUMA DRESSINGLevtrade Intl. (Pty) , Ltd.K926290BURN SHEETGam Industries, Inc.K900441BURNS CASUALTY SHEETPilgrim Medical ServicesK900442BURNS CASUALTY SHEET BURN ROLLPilgrim Medical Services

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.

↑