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FDA 510(k)

SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE

K-Number: K872906 · 1987-08-11

ApplicantAmerican Silk Sutures, Inc.
Decision Date1987-08-11
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE is the device name listed in this FDA 510(k) record. The listed applicant is American Silk Sutures, Inc.. It received FDA 510(k) clearance on 1987-08-11 under 510(k) number K872906. 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 SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE?

SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE is a medical device that received FDA 510(k) clearance on 1987-08-11. The listed applicant is American Silk Sutures, Inc.. The 510(k) number is K872906.

When did SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE receive FDA 510(k) clearance?

SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE received FDA 510(k) clearance on 1987-08-11, under 510(k) number K872906.

Who is the listed applicant for SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE?

The FDA 510(k) record lists American Silk Sutures, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE?

The FDA product code for SUCTION TUBE TIP FITS OVER BUSSIE FRAZIER TUBE is GEA.

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Other records listing American Silk Sutures, Inc. as applicant

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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

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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