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FDA 510(k)

SURGICAL SUCTION APPARATUS

K-Number: K895670 · 1989-09-27

ApplicantBaker-Sundt Research, Inc.
Decision Date1989-09-27
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL SUCTION APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is Baker-Sundt Research, Inc.. It received FDA 510(k) clearance on 1989-09-27 under 510(k) number K895670. 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 SURGICAL SUCTION APPARATUS?

SURGICAL SUCTION APPARATUS is a medical device that received FDA 510(k) clearance on 1989-09-27. The listed applicant is Baker-Sundt Research, Inc.. The 510(k) number is K895670.

When did SURGICAL SUCTION APPARATUS receive FDA 510(k) clearance?

SURGICAL SUCTION APPARATUS received FDA 510(k) clearance on 1989-09-27, under 510(k) number K895670.

Who is the listed applicant for SURGICAL SUCTION APPARATUS?

The FDA 510(k) record lists Baker-Sundt Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL SUCTION APPARATUS?

The FDA product code for SURGICAL SUCTION APPARATUS is GEA.

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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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