INAMED PRO-TEC SILICONE SURGICAL GLOVES— 510(k) K894073

Substantially Equivalent

Inamed Development Co.

FDA 510(k) clearance K894073 for INAMED PRO-TEC SILICONE SURGICAL GLOVES, Substantially Equivalent on 1989-09-18. Applicant: Inamed Development Co.. Device class: 1.

Clearance details

Applicant
Inamed Development Co.
Product code
Code KGO
Device class
Class 1
Regulation
21 CFR 878.4460
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Carpinteria, CA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code KGO

view all

More clearances from Inamed Development Co.

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.