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FDA 510(k)

MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP

K-Number: K915353 · 1991-12-27

ApplicantMatrix Medica, Inc.
Decision Date1991-12-27
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP 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 1991-12-27 under 510(k) number K915353. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP?

MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP is a medical device that received FDA 510(k) clearance on 1991-12-27. The listed applicant is Matrix Medica, Inc.. The 510(k) number is K915353.

When did MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP receive FDA 510(k) clearance?

MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP received FDA 510(k) clearance on 1991-12-27, under 510(k) number K915353.

Who is the listed applicant for MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP?

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 MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP?

The FDA product code for MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP is EIA.

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Related Devices (Code: EIA)

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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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