Last synced on 20 December 2024 at 11:05 pm

HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101538
510(k) Type
Traditional
Applicant
PHILIPS ELECTRONICS UK LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/5/2010
Days to Decision
155 days
Submission Type
Summary

HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101538
510(k) Type
Traditional
Applicant
PHILIPS ELECTRONICS UK LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/5/2010
Days to Decision
155 days
Submission Type
Summary