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FDA 510(k)

TURKEL THORACENTESIS NEEDLE

K-Number: K921461 · 1992-07-30

ApplicantSymbiosis Corp.
Decision Date1992-07-30
Product CodeGSS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TURKEL THORACENTESIS NEEDLE 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 K921461. The device is classified under product code GSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURKEL THORACENTESIS NEEDLE?

TURKEL THORACENTESIS NEEDLE 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 K921461.

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

TURKEL THORACENTESIS NEEDLE received FDA 510(k) clearance on 1992-07-30, under 510(k) number K921461.

Who is the listed applicant for TURKEL THORACENTESIS NEEDLE?

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 NEEDLE?

The FDA product code for TURKEL THORACENTESIS NEEDLE is GSS.

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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

View all 34 devices →

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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