ClearanceBrief
Company ยท US

Ercons, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 1999. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LKYDevice, External Penile Rigidity6

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 24, 1999K990008ERCO-RIBBON -C
Ercons, Inc.
LKY
Feb 24, 1999K990006ERCO-VAC -C
Ercons, Inc.
LKY
Nov 24, 1998K981357ERCO-VAC
Ercons, Inc.
LKY
Nov 24, 1998K981343ERCO-RIBBON
Ercons, Inc.
LKY
Nov 3, 1997K972537ERCO-VAC
Ercons, Inc.
LKY
Oct 28, 1997K972353ERCO-RIBBON
Ercons, Inc.
LKY

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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