FDA.reportPublic FDA data

510(k) K772188

Device
Fsh Ria Kit (125i)
Applicant
DIAGNOSTIC PRODUCTS CORP.
510(k) number
K772188
Product code
FSH
Decision
Substantially Equivalent (SESE)
Decision date
1977-12-22
Date received
1977-11-25
Regulation
878.4800
Classification name
Tray, Surgical, Needle
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
4221 Richmond Rd., NW Walker MI US 49534 49534

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FSH#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K884876S 4 INSTRUMENT STANDCarl Zeiss, Inc.1988-12-15
K883578S 21 INSTRUMENT STANDCarl Zeiss, Inc.1988-09-13
K821921STAND, SURG. INSTRUMENT & DRESSINGEmerson-Sack-Warner Corp.1982-07-30
K813337SKINNY CHIBA NEEDLE & TRAYAmerican Pharmaseal Div. Ahsc1982-01-28
K813338BIOPSY NEEDLES & TRAYSAmerican Pharmaseal Div. Ahsc1982-01-28
K813335PERCUTANEOUS TRANSHEPATIC CHOLANG. TRAYAmerican Pharmaseal Div. Ahsc1982-01-08
K780759MODEL 902 STANDApplied Medical Research1978-05-19