Integrated Medical Systems, Inc.
Integrated Medical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 2008, with 22 FDA device recalls on record.
Top product codes for Integrated Medical Systems, Inc.
FDA recalls by Integrated Medical Systems, Inc.
10 most recent of 22- Z-0890-2016 — Olympus, Model No. GIF-H180, flexible scope, large diameter, video gastroscope
- Z-0904-2016 — Olympus, Model No. GIF-Q160, flexible scope, large diameter, video gastroscope
- Z-0896-2016 — Olympus, Model No. CF-Q180AL, flexible scope, large diameter, video colonoscope
- Z-0902-2016 — Olympus, Model No. CF-Q160AL, flexible scope, large diameter, video colonoscope
- Z-0893-2016 — Olympus, Model No. GIF-H180J, flexible scope, large diameter, video gastroscope
- Z-0894-2016 — Olympus, Model No. GIF-Q180,flexible scope, large diameter, video gastroscope
- Z-0908-2016 — Olympus, Model No. PCF-H190L, flexible scope, large diameter, video pediatric colonoscope
- Z-0905-2016 — Olympus, Model No. TJF-160F, flexible scope, large diameter, video duodenoscope
- Z-0901-2016 — Olympus, Model No. PCF-Q180AL, flexible scope, large diameter, video colonoscope
- Z-0910-2016 — Olympus, Model No. XCF-Q160ALE, flexible scope, large diameter, video colonoscope
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Integrated Medical Systems, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.