ClearanceBrief
Company ยท US

American Laser Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 2001. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEXPowered Laser Surgical Instrument2
HPJInstrument, Visual Field, Laser1
HQFLaser, Ophthalmic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 5, 2001K010046NUVOLASE 532 MEDICAL LASER SYSTEM
American Laser Corp.
GEX
May 17, 1999K990665BQ/BM INTEGRATED LASER DELIVERY SYSTEM
American Laser Corp.
HQF
Mar 22, 1999K990725NUVOLASE 532 LASER SYSTEM
American Laser Corp.
GEX
Jan 7, 1983K827819LASER PHOTOCOAGULATOR
American Laser Corp.
Jan 22, 1982K813429LASER PHOTOCOAGULATOR ARGON MED. LASER
American Laser Corp.
HPJ

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes