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FDA 510(k)

EXPRESSE AND PREMIER POWERED BREAST PUMPS

K-Number: K973501 · 1997-12-11

Decision Date1997-12-11
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EXPRESSE AND PREMIER POWERED BREAST PUMPS is the device name listed in this FDA 510(k) record. The listed applicant is Ameda Medizintechnik AG. It received FDA 510(k) clearance on 1997-12-11 under 510(k) number K973501. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPRESSE AND PREMIER POWERED BREAST PUMPS?

EXPRESSE AND PREMIER POWERED BREAST PUMPS is a medical device that received FDA 510(k) clearance on 1997-12-11. The listed applicant is Ameda Medizintechnik AG. The 510(k) number is K973501.

When did EXPRESSE AND PREMIER POWERED BREAST PUMPS receive FDA 510(k) clearance?

EXPRESSE AND PREMIER POWERED BREAST PUMPS received FDA 510(k) clearance on 1997-12-11, under 510(k) number K973501.

Who is the listed applicant for EXPRESSE AND PREMIER POWERED BREAST PUMPS?

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

What is the FDA product code for EXPRESSE AND PREMIER POWERED BREAST PUMPS?

The FDA product code for EXPRESSE AND PREMIER POWERED BREAST PUMPS is HGX.

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.

Related Devices (Code: HGX)

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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