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FDA 510(k)

CURASALT HYPERTONIC SALINE DRESSING

K-Number: K942459 · 1994-06-27

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1994-06-27
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CURASALT HYPERTONIC SALINE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1994-06-27 under 510(k) number K942459. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURASALT HYPERTONIC SALINE DRESSING?

CURASALT HYPERTONIC SALINE DRESSING is a medical device that received FDA 510(k) clearance on 1994-06-27. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K942459.

When did CURASALT HYPERTONIC SALINE DRESSING receive FDA 510(k) clearance?

CURASALT HYPERTONIC SALINE DRESSING received FDA 510(k) clearance on 1994-06-27, under 510(k) number K942459.

Who is the listed applicant for CURASALT HYPERTONIC SALINE DRESSING?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURASALT HYPERTONIC SALINE DRESSING?

The FDA product code for CURASALT HYPERTONIC SALINE DRESSING is KMF.

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Other records listing Kendall Healthcare Products Co. Div.Of Tyco Health 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.

K973763KENDALL CURITY IODOFORM PACKING STRIPK973511KENDALL CURITY PETROLATUM GAUZEK973507KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)K973619KENDALL CURITY NON-ADHERING DRESSINGK973509KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSINGK973546KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER

View all 66 devices →

Related Devices (Code: KMF)

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.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, 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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