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FDA 510(k)

PRO-TECT TRAUMA PAK

K-Number: K941789 · 1995-01-12

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

Device Summary

PRO-TECT TRAUMA PAK 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 K941789. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-TECT TRAUMA PAK?

PRO-TECT TRAUMA PAK 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 K941789.

When did PRO-TECT TRAUMA PAK receive FDA 510(k) clearance?

PRO-TECT TRAUMA PAK received FDA 510(k) clearance on 1995-01-12, under 510(k) number K941789.

Who is the listed applicant for PRO-TECT TRAUMA PAK?

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 TRAUMA PAK?

The FDA product code for PRO-TECT TRAUMA PAK 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.

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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.

K941790PRO-TECT SAFETY DRESSING

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

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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