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PACEMAKER HIGH-SPEED HANDPIECE MODEL PM-MQ, PM-M

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101551
510(k) Type
Traditional
Applicant
DELMA MEDICAL INSTRUMENT (GUANGZHOU) CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2010
Days to Decision
97 days
Submission Type
Summary

PACEMAKER HIGH-SPEED HANDPIECE MODEL PM-MQ, PM-M

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101551
510(k) Type
Traditional
Applicant
DELMA MEDICAL INSTRUMENT (GUANGZHOU) CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2010
Days to Decision
97 days
Submission Type
Summary