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FDA 510(k)

MATRIX DRI-IDEA BOOTIES

K-Number: K850661 · 1985-03-11

ApplicantMatrix Medica, Inc.
Decision Date1985-03-11
Product Code
DecisionSubstantially Equivalent

Device Summary

MATRIX DRI-IDEA BOOTIES is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Medica, Inc.. It received FDA 510(k) clearance on 1985-03-11 under 510(k) number K850661. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRIX DRI-IDEA BOOTIES?

MATRIX DRI-IDEA BOOTIES is a medical device that received FDA 510(k) clearance on 1985-03-11. The listed applicant is Matrix Medica, Inc.. The 510(k) number is K850661.

When did MATRIX DRI-IDEA BOOTIES receive FDA 510(k) clearance?

MATRIX DRI-IDEA BOOTIES received FDA 510(k) clearance on 1985-03-11, under 510(k) number K850661.

Who is the listed applicant for MATRIX DRI-IDEA BOOTIES?

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

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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.

K961536FLEXSCOPEK923693KLORMANK921982MATRX HOPE(R) 5 RESUSCITATORK915353MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMPK912661MATRX, PYRAMID TRIANGLE BANDAGEK900551MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.

View all 14 devices →

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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