MATRX, PYRAMID TRIANGLE BANDAGE
K-Number: K912661 · 1991-08-21
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Device Summary
Frequently Asked Questions
What is the MATRX, PYRAMID TRIANGLE BANDAGE?
MATRX, PYRAMID TRIANGLE BANDAGE is a medical device that received FDA 510(k) clearance on 1991-08-21. The listed applicant is Matrix Medica, Inc.. The 510(k) number is K912661.
When did MATRX, PYRAMID TRIANGLE BANDAGE receive FDA 510(k) clearance?
MATRX, PYRAMID TRIANGLE BANDAGE received FDA 510(k) clearance on 1991-08-21, under 510(k) number K912661.
Who is the listed applicant for MATRX, PYRAMID TRIANGLE BANDAGE?
The FDA 510(k) record lists Matrix Medica, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MATRX, PYRAMID TRIANGLE BANDAGE?
The FDA product code for MATRX, PYRAMID TRIANGLE BANDAGE is ILI.
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.
Other records listing Matrix Medica, 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.
Related Devices (Code: ILI)
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.
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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