Last synced on 19 July 2024 at 11:05 pm

MICROJET CAVITY PREPARATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964755
510(k) Type
Traditional
Applicant
MIDWEST DENTAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1997
Days to Decision
288 days
Submission Type
Statement

MICROJET CAVITY PREPARATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964755
510(k) Type
Traditional
Applicant
MIDWEST DENTAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1997
Days to Decision
288 days
Submission Type
Statement