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FDA 510(k)

MICREL LTD PORTABLE INFUSION MICROPUMP

K-Number: K903571 · 1991-02-01

Decision Date1991-02-01
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICREL LTD PORTABLE INFUSION MICROPUMP is the device name listed in this FDA 510(k) record. The listed applicant is Technology Transfer Intl., Inc.. It received FDA 510(k) clearance on 1991-02-01 under 510(k) number K903571. 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 MICREL LTD PORTABLE INFUSION MICROPUMP?

MICREL LTD PORTABLE INFUSION MICROPUMP is a medical device that received FDA 510(k) clearance on 1991-02-01. The listed applicant is Technology Transfer Intl., Inc.. The 510(k) number is K903571.

When did MICREL LTD PORTABLE INFUSION MICROPUMP receive FDA 510(k) clearance?

MICREL LTD PORTABLE INFUSION MICROPUMP received FDA 510(k) clearance on 1991-02-01, under 510(k) number K903571.

Who is the listed applicant for MICREL LTD PORTABLE INFUSION MICROPUMP?

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

What is the FDA product code for MICREL LTD PORTABLE INFUSION MICROPUMP?

The FDA product code for MICREL LTD PORTABLE INFUSION MICROPUMP is FRN.

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 Technology Transfer Intl., 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: FRN)

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

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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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