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Fisher Imaging Corp. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Fisher Imaging Corp. has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Fisher Imaging Corp." is on file.

What these totals cover: FDA records filed under the name "Fisher Imaging Corp." and its spelling variant "Fisher Imaging".

Latest 510(k): Jun 16, 1995

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	3	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	0	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

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Recent 510(k) clearances

3 510(k) clearances from Jan 16, 1986 to Jun 16, 1995.

K-Number	Device	Date
K952456	IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM	Jun 16, 1995
K870783	BPA CARDIOVASCULAR PRESSURE AMPLIFIER	Apr 27, 1987
K853652	BERS-400A ELECTROPHYSIOLOGICAL AMPLIFIERS & INPUT	Jan 16, 1986

Fisher Imaging Corp. and the FDA: common questions

Has Fisher Imaging Corp. received an FDA warning letter?

No FDA warning letter addressed to the name "Fisher Imaging Corp." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Fisher Imaging Corp. received an FDA Form 483?

FDA has not published a Form 483 for "Fisher Imaging Corp." in its reading room. FDA publishes some Form 483s, not all of them.

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