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FDA 510(k)

PRO-TECT SAFETY DRESSING

K-Number: K941790 · 1995-01-12

ApplicantPro-Tect Medical Products, Inc.
Decision Date1995-01-12
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

PRO-TECT SAFETY DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Tect Medical Products, Inc.. It received FDA 510(k) clearance on 1995-01-12 under 510(k) number K941790. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-TECT SAFETY DRESSING?

PRO-TECT SAFETY DRESSING is a medical device that received FDA 510(k) clearance on 1995-01-12. The listed applicant is Pro-Tect Medical Products, Inc.. The 510(k) number is K941790.

When did PRO-TECT SAFETY DRESSING receive FDA 510(k) clearance?

PRO-TECT SAFETY DRESSING received FDA 510(k) clearance on 1995-01-12, under 510(k) number K941790.

Who is the listed applicant for PRO-TECT SAFETY DRESSING?

The FDA 510(k) record lists Pro-Tect Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRO-TECT SAFETY DRESSING?

The FDA product code for PRO-TECT SAFETY DRESSING is MGP.

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 Pro-Tect Medical Products, 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.

K941789PRO-TECT TRAUMA PAK

Related Devices (Code: MGP)

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.

K012995COLLATEK SHEETBiocore Medical Technologies, Inc.K012997COLLATEK FOAMBiocore Medical Technologies, Inc.K001508LASERSKIN DRESSINGFidia Advanced Biopolymers SrlK990079FASTSEAL CHEST WOUND DRESSINGGreenfield Medical Technologies, Inc.K991214SIMPLICARE TRANSPARENT WOUND DRESSINGHollister, Inc.K992302DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORSDermaphylyx, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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