Last synced on 30 May 2025 at 11:05 pm

REDI-CHECK PHOTMETER Q.A.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923598
510(k) Type
Traditional
Applicant
AWARENESS TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1992
Days to Decision
86 days
Submission Type
Statement

REDI-CHECK PHOTMETER Q.A.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923598
510(k) Type
Traditional
Applicant
AWARENESS TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1992
Days to Decision
86 days
Submission Type
Statement