ClearanceBrief
Company ยท US

Portlyn Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1997. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DWZDevice, Biopsy, Endomyocardial2
FCLForceps, Biopsy, Non-Electric2
HETLaparoscope, Gynecologic (And Accessories)2
EOQBronchoscope (Flexible Or Rigid)1
KGEForceps, Biopsy, Electric1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 17, 1997K970083DYNABITE HOT GI BIOPSY FORCEPS
Portlyn Corp.
KGE
Jul 27, 1995K951447DYNABITE CARDIOVASCULAR BIOPSY FORCEPS
Portlyn Corp.
DWZ
Jun 1, 1995K952391DYNABITE UROLOGICAL FORCEPS
Portlyn Corp.
FCL
Nov 15, 1994K944245DYNABITE LAPAROSCOPIC FORCEPS
Portlyn Corp.
HET
Mar 22, 1994K934506DYNABITE HYSTEROSCOPIC FORCEPS
Portlyn Corp.
HET
Jun 29, 1990K901300BIOPSY FORCEPS
Portlyn Corp.
DWZ
Apr 16, 1990K896147BIOPSY FORCEP (NON-ELECTRIC)
Portlyn Corp.
FCL
Mar 9, 1990K896146BIOPSY FORCEPS, (NON-RIGID)
Portlyn Corp.
EOQ

Latest recalls

DateFirm and productCodeLinked 510(k)
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