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FDA 510(k)

MEDELA CLARIO HOME CARE PUMP

K-Number: K033179 · 2003-10-15

ApplicantMedela AG
Decision Date2003-10-15
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDELA CLARIO HOME CARE PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Medela AG. It received FDA 510(k) clearance on 2003-10-15 under 510(k) number K033179. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDELA CLARIO HOME CARE PUMP?

MEDELA CLARIO HOME CARE PUMP is a medical device that received FDA 510(k) clearance on 2003-10-15. The listed applicant is Medela AG. The 510(k) number is K033179.

When did MEDELA CLARIO HOME CARE PUMP receive FDA 510(k) clearance?

MEDELA CLARIO HOME CARE PUMP received FDA 510(k) clearance on 2003-10-15, under 510(k) number K033179.

Who is the listed applicant for MEDELA CLARIO HOME CARE PUMP?

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

What is the FDA product code for MEDELA CLARIO HOME CARE PUMP?

The FDA product code for MEDELA CLARIO HOME CARE PUMP is BTA.

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 Medela AG 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.

View all 23 devices →

Related Devices (Code: BTA)

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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