Last synced on 27 January 2023 at 11:04 pm

MICROSPEARS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780257
510(k) Type
Traditional
Applicant
SPARTA INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1978
Days to Decision
8 days

MICROSPEARS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780257
510(k) Type
Traditional
Applicant
SPARTA INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1978
Days to Decision
8 days