ClearanceBrief
Company ยท US

Gamp & Assoc.

FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 1996. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MPAEndoilluminator5
HQBPhotocoagulator And Accessories3
HQRApparatus, Cautery, Radiofrequency, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 5, 1996K952585GAMP & ASSOCIATES DISPOSABLE END IRRIGATING ENDOILLUMINATOR
Gamp & Assoc.
MPA
Jan 5, 1996K952581GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC VISCOINJECTOR
Gamp & Assoc.
MPA
Jan 5, 1996K952569GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR
Gamp & Assoc.
HQR
Dec 22, 1995K954308GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE
Gamp & Assoc.
HQB
Dec 22, 1995K954307GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE
Gamp & Assoc.
HQB
Dec 22, 1995K954306GAMP & ASSOC. DISPOSABLE ILL ENDOCULAR LASER PROBE
Gamp & Assoc.
HQB
Sep 1, 1995K952586GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC ENDOILLUMINATOR
Gamp & Assoc.
MPA
Sep 1, 1995K952584GAMP & ASSOCIATES DISPOSABLE ENDOILLUMINATOR W/PICK
Gamp & Assoc.
MPA
Sep 1, 1995K952580GAMP & ASSOCIATES DISPOSABLE BARE END FIBER
Gamp & Assoc.
MPA

Latest recalls

DateFirm and productCodeLinked 510(k)
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