TURKEL THORACENTESIS NEEDLE— 510(k) K921461

Substantially Equivalent

Symbiosis Corp.

FDA 510(k) clearance K921461 for TURKEL THORACENTESIS NEEDLE, Substantially Equivalent on 1992-07-30. Applicant: Symbiosis Corp.. Device class: 2.

Clearance details

Applicant: Symbiosis Corp.
Product code: Code GSS
Device class: Class 2
Regulation: 21 CFR 866.3415
Advisory panel: Microbiology
Date received: 1992-03-27
Decision date: 1992-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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K953453 — SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES1996-01-17
K953242 — SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES1995-10-06
K952432 — SYMBIOSIS BIPOLAR FORCEPS1995-07-05
K951387 — SYMBIOSIS BIPOLAR SCISSORS1995-04-10

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