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FDA 510(k)

CURITY CURAD BANDAGES

K-Number: K810126 · 1981-02-06

ApplicantThe Kendal Co.
Decision Date1981-02-06
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CURITY CURAD BANDAGES 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 1981-02-06 under 510(k) number K810126. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY CURAD BANDAGES?

CURITY CURAD BANDAGES is a medical device that received FDA 510(k) clearance on 1981-02-06. The listed applicant is The Kendal Co.. The 510(k) number is K810126.

When did CURITY CURAD BANDAGES receive FDA 510(k) clearance?

CURITY CURAD BANDAGES received FDA 510(k) clearance on 1981-02-06, under 510(k) number K810126.

Who is the listed applicant for CURITY CURAD BANDAGES?

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 CURITY CURAD BANDAGES?

The FDA product code for CURITY CURAD BANDAGES is KGX.

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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

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Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, 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.

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