Last synced on 14 November 2025 at 11:06 pm

PERFECTEMP OPHTHALMIC CAUTERY

Page Type
Cleared 510(K)
510(k) Number
K801078
510(k) Type
Traditional
Applicant
MEDICAL PRODUCTS DEVELOPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
28 days

PERFECTEMP OPHTHALMIC CAUTERY

Page Type
Cleared 510(K)
510(k) Number
K801078
510(k) Type
Traditional
Applicant
MEDICAL PRODUCTS DEVELOPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
28 days