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)

DERMAGRAN WET DRESSING (ZINC-SALINE)

K-Number: K913344 · 1992-07-14

ApplicantDerma Sciences, Inc.
Decision Date1992-07-14
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

DERMAGRAN WET DRESSING (ZINC-SALINE) 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 1992-07-14 under 510(k) number K913344. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMAGRAN WET DRESSING (ZINC-SALINE)?

DERMAGRAN WET DRESSING (ZINC-SALINE) is a medical device that received FDA 510(k) clearance on 1992-07-14. The listed applicant is Derma Sciences, Inc.. The 510(k) number is K913344.

When did DERMAGRAN WET DRESSING (ZINC-SALINE) receive FDA 510(k) clearance?

DERMAGRAN WET DRESSING (ZINC-SALINE) received FDA 510(k) clearance on 1992-07-14, under 510(k) number K913344.

Who is the listed applicant for DERMAGRAN WET DRESSING (ZINC-SALINE)?

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 WET DRESSING (ZINC-SALINE)?

The FDA product code for DERMAGRAN WET DRESSING (ZINC-SALINE) is MGQ.

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 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

View all 20 devices →

Related Devices (Code: MGQ)

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.

K171879HylaGuard Moisturizing CreamFounders Science Group, LLCK083024HYLATOPIC EMOLLIENT FOAMCollegium Pharmaceutical IncorporatedK041342IMPRUV A.I. CREAM WOUND AND SKIN EMULSIONStiefel Laboratories, Inc.K041268SILVERSITE OR CALGITROLAdriK040019SILVERSEALNoble Fiber TechnologiesK040517TENDERWET ACTIVEMedline Industries, 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.

↑