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)

B. BRAUN MEDICAL INC. TRANSORBENT AND THINSITE BORDER DRESSING

K-Number: K970453 · 1997-04-11

ApplicantB.Braun Medical, Inc.
Decision Date1997-04-11
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

B. BRAUN MEDICAL INC. TRANSORBENT AND THINSITE BORDER DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 1997-04-11 under 510(k) number K970453. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the B. BRAUN MEDICAL INC. TRANSORBENT AND THINSITE BORDER DRESSING?

B. BRAUN MEDICAL INC. TRANSORBENT AND THINSITE BORDER DRESSING is a medical device that received FDA 510(k) clearance on 1997-04-11. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K970453.

When did B. BRAUN MEDICAL INC. TRANSORBENT AND THINSITE BORDER DRESSING receive FDA 510(k) clearance?

B. BRAUN MEDICAL INC. TRANSORBENT AND THINSITE BORDER DRESSING received FDA 510(k) clearance on 1997-04-11, under 510(k) number K970453.

Who is the listed applicant for B. BRAUN MEDICAL INC. TRANSORBENT AND THINSITE BORDER DRESSING?

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

What is the FDA product code for B. BRAUN MEDICAL INC. TRANSORBENT AND THINSITE BORDER DRESSING?

The FDA product code for B. BRAUN MEDICAL INC. TRANSORBENT AND THINSITE BORDER DRESSING 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 B.Braun Medical, 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.

K254111Irrigation/Urology SetsK253235Introcan Safety® Deep Access XL IV CatheterK243392Infusomat® Space Volumetric Infusion Pump Administration SetsK240578VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter SystemK241845Introcan Safety® 2 IV CatheterK241385Omnifix Syringe NRFit

View all 142 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.

↑