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FDA 510(k)

TURKEL THORACENTESIS SYSTEM

K-Number: K922614 · 1992-07-30

ApplicantSymbiosis Corp.
Decision Date1992-07-30
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TURKEL THORACENTESIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1992-07-30 under 510(k) number K922614. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURKEL THORACENTESIS SYSTEM?

TURKEL THORACENTESIS SYSTEM is a medical device that received FDA 510(k) clearance on 1992-07-30. The listed applicant is Symbiosis Corp.. The 510(k) number is K922614.

When did TURKEL THORACENTESIS SYSTEM receive FDA 510(k) clearance?

TURKEL THORACENTESIS SYSTEM received FDA 510(k) clearance on 1992-07-30, under 510(k) number K922614.

Who is the listed applicant for TURKEL THORACENTESIS SYSTEM?

The FDA 510(k) record lists Symbiosis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TURKEL THORACENTESIS SYSTEM?

The FDA product code for TURKEL THORACENTESIS SYSTEM is GAA.

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Other records listing Symbiosis Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953453SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODESK952432SYMBIOSIS BIPOLAR FORCEPSK951387SYMBIOSIS BIPOLAR SCISSORSK950286SYMBIOSIS BIPOLAR SCISSORS

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Related Devices (Code: GAA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K223625CapnoSpot™ Pneumothorax Decompression IndicatorPneumeric, Inc.K102274ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTArvik Enterprises/ Mini Lap TechnologiesK011586IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGEDiametrics Medical, Inc.K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESXimed/Prosure/InjectxK983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXXimed/Prosure/InjectxK974741MANAN ACCURA NEEDLEMedical Device Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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