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FDA 510(k)

CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC

K-Number: K895762 · 1989-10-18

ApplicantKolster Methods
Decision Date1989-10-18
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC is the device name listed in this FDA 510(k) record. The listed applicant is Kolster Methods. It received FDA 510(k) clearance on 1989-10-18 under 510(k) number K895762. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC?

CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC is a medical device that received FDA 510(k) clearance on 1989-10-18. The listed applicant is Kolster Methods. The 510(k) number is K895762.

When did CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC receive FDA 510(k) clearance?

CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC received FDA 510(k) clearance on 1989-10-18, under 510(k) number K895762.

Who is the listed applicant for CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC?

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

What is the FDA product code for CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC?

The FDA product code for CANULA SUCTION FOR SURGICAL GENERAL AND PLASTIC is GEA.

Related Clinical Trials

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Other records listing Kolster Methods 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.

K935820KOLSTER METHODSK895761GENERAL ASPERATOR

Related Devices (Code: GEA)

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.

K003965MRI SAFE INSTRUMENTSAesculap, Inc.K982472GENICON TROCARGenicon, LCK954599CONMED TROGARD ELECTRONIC TROCAR SYSTEMConmedcorpK922460ORIGIN SECONDARY CANNULA AND TROCAROrigin Medsystems, Inc.K920110ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVEETHICON, Inc.K911262DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCERETHICON, Inc.

Official Source

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

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