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FDA 510(k)

DYNASORB

K-Number: K951561 · 1995-09-01

ApplicantDermarx Corp.
Decision Date1995-09-01
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DYNASORB is the device name listed in this FDA 510(k) record. The listed applicant is Dermarx Corp.. It received FDA 510(k) clearance on 1995-09-01 under 510(k) number K951561. 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 DYNASORB?

DYNASORB is a medical device that received FDA 510(k) clearance on 1995-09-01. The listed applicant is Dermarx Corp.. The 510(k) number is K951561.

When did DYNASORB receive FDA 510(k) clearance?

DYNASORB received FDA 510(k) clearance on 1995-09-01, under 510(k) number K951561.

Who is the listed applicant for DYNASORB?

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

What is the FDA product code for DYNASORB?

The FDA product code for DYNASORB is KMF.

Related Clinical Trials

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Other records listing Dermarx Corp. 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.

K972336DERMAMEND HYDROGEL GAUZE DRESSINGK970600DERMAMEND FOAM ISLAND DRESSINGK962089DERMAMEND GEL

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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