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FDA 510(k)

DERMAGRAN HYDROPHILIC OINTMENT

K-Number: K951499 · 1995-04-18

ApplicantDerma Sciences, Inc.
Decision Date1995-04-18
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMAGRAN HYDROPHILIC OINTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Derma Sciences, Inc.. It received FDA 510(k) clearance on 1995-04-18 under 510(k) number K951499. 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 DERMAGRAN HYDROPHILIC OINTMENT?

DERMAGRAN HYDROPHILIC OINTMENT is a medical device that received FDA 510(k) clearance on 1995-04-18. The listed applicant is Derma Sciences, Inc.. The 510(k) number is K951499.

When did DERMAGRAN HYDROPHILIC OINTMENT receive FDA 510(k) clearance?

DERMAGRAN HYDROPHILIC OINTMENT received FDA 510(k) clearance on 1995-04-18, under 510(k) number K951499.

Who is the listed applicant for DERMAGRAN HYDROPHILIC OINTMENT?

The FDA 510(k) record lists Derma Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DERMAGRAN HYDROPHILIC OINTMENT?

The FDA product code for DERMAGRAN HYDROPHILIC OINTMENT is KMF.

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Other records listing Derma Sciences, Inc. 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.

K110546MEDIHONEY HYDROGEL SHEET DRESSINGS WITH ACTIVE LEPTOSPERMUM HONEYK101793MEDIHONEY GEL DRESSING WITH ACTIVE MANUKA HONEYK081584DERMA SCIENCES OTC MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEYK080315DERMA SCIENCES MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEYK072956MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEYK970660DERMAGRAN WOUND MANAGEMENT SYSTEM

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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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