JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETER— 510(k) K872917

Name: FDA 510(k) clearance K872917
Creator: U.S. Food and Drug Administration
Published: 1987-08-11

Substantially Equivalent

American Pharmaseal Div. Ahsc

FDA 510(k) clearance K872917 for JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETER, Substantially Equivalent on 1987-08-11. Applicant: American Pharmaseal Div. Ahsc. Device class: 1.

Clearance details

Applicant: American Pharmaseal Div. Ahsc
Product code: Code BSY
Device class: Class 1
Regulation: 21 CFR 868.6810
Advisory panel: Anesthesiology
Date received: 1987-07-27
Decision date: 1987-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valencia, CA, US

Download summary PDF View on FDA.gov ↗

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K992902 — AMBU HAND POWER SUCTION PUMP1999-10-25
K982945 — DUAL PURPOSE CLOSED CATHETER1998-09-22
K981910 — SUCTION CATHETER1998-08-24
K972258 — HI-CARE CLOSED SUCTION SYSTEM1997-12-29

More clearances from American Pharmaseal Div. Ahsc

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K874022 — PHARMASEAL WOUND IRRIGATION DEVICE1987-12-30
K874045 — PHARMASEAL ENDOSCOPY PREP KIT UPPER AND LOWER1987-12-03
K874517 — PHARMASEAL RUBBER URETHRAL CATHETER1987-12-03
K873359 — AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE1987-11-06
K872228 — PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM1987-09-04

Adverse events under product code BSY

product code BSY

Death: 3
Injury: 155
Malfunction: 959
Total: 1,117

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.