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FDA 510(k)

TURKEL ABDOMINAL PARACENTESIS SYSTEM

K-Number: K924702 · 1993-01-12

ApplicantSymbiosis Corp.
Decision Date1993-01-12
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TURKEL ABDOMINAL PARACENTESIS 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 1993-01-12 under 510(k) number K924702. The device is classified under product code GBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURKEL ABDOMINAL PARACENTESIS SYSTEM?

TURKEL ABDOMINAL PARACENTESIS SYSTEM is a medical device that received FDA 510(k) clearance on 1993-01-12. The listed applicant is Symbiosis Corp.. The 510(k) number is K924702.

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

TURKEL ABDOMINAL PARACENTESIS SYSTEM received FDA 510(k) clearance on 1993-01-12, under 510(k) number K924702.

Who is the listed applicant for TURKEL ABDOMINAL PARACENTESIS 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 ABDOMINAL PARACENTESIS SYSTEM?

The FDA product code for TURKEL ABDOMINAL PARACENTESIS SYSTEM is GBX.

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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: GBX)

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.

K082725GRAFTGUARD PRESSURE CONTROLLING SYRINGEMaquet Cardiovascular, LLCK052286DEUTSCH ANTI-BLOCKAGE WOUND DRAINThe Catheter Exchange, Inc.K043515GRAFTSAVERVescare, Inc.K013417MISONIX IRRIGATION SYSTEM MOEDL BC20PMisonix, Inc.K000704DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)Dmc Medical, Ltd.K974233LYSONIX IRRIGATION SYSTEMLysonix, 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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