ClearanceBrief
Company ยท US

Aesthetech Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1987. 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
BTAPump, Portable, Aspiration (Manual Or Powered)1
FWPProsthesis, Chin, Internal1
HQCUnit, Phacofragmentation1
LCJTissue Expander And Accessories1
LZKImplant, Malar1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 25, 1987K873940CREAT BRAND O-RISE GENERAL ASPIRATOR
Aesthetech Corp.
BTA
Sep 11, 1987K873434CREAT BRAND MALAR IMPLANT
Aesthetech Corp.
LZK
Sep 24, 1985K853189CREAT BRAND I/A PACK CREAT BRAND PHACO PACK
Aesthetech Corp.
HQC
Nov 6, 1984K843678CREAT BRAND SKIN EXPANDER
Aesthetech Corp.
LCJ
Apr 24, 1984K841283DISPOSABLE SUCTION TUBING SET
Aesthetech Corp.
Sep 11, 1981K812210CREAT BRAND WAGNER CHIN IMPLANT
Aesthetech Corp.
FWP

Latest recalls

DateFirm and productCodeLinked 510(k)
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