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FDA 510(k)

PHARMETRIX MINIPUMP MODEL 5120

K-Number: K924603 · 1994-03-31

ApplicantPharmetrix, Inc.
Decision Date1994-03-31
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHARMETRIX MINIPUMP MODEL 5120 is the device name listed in this FDA 510(k) record. The listed applicant is Pharmetrix, Inc.. It received FDA 510(k) clearance on 1994-03-31 under 510(k) number K924603. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARMETRIX MINIPUMP MODEL 5120?

PHARMETRIX MINIPUMP MODEL 5120 is a medical device that received FDA 510(k) clearance on 1994-03-31. The listed applicant is Pharmetrix, Inc.. The 510(k) number is K924603.

When did PHARMETRIX MINIPUMP MODEL 5120 receive FDA 510(k) clearance?

PHARMETRIX MINIPUMP MODEL 5120 received FDA 510(k) clearance on 1994-03-31, under 510(k) number K924603.

Who is the listed applicant for PHARMETRIX MINIPUMP MODEL 5120?

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

What is the FDA product code for PHARMETRIX MINIPUMP MODEL 5120?

The FDA product code for PHARMETRIX MINIPUMP MODEL 5120 is FRN.

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Other records listing Pharmetrix, 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.

K915407PHARMETRIX MEDIPUMP MODEL 524

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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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