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FDA 510(k)

SUCTION TUBE

K-Number: K864770 · 1987-02-24

ApplicantNew England Surgical Instrument Corp.
Decision Date1987-02-24
Product CodeFFA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SUCTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is New England Surgical Instrument Corp.. It received FDA 510(k) clearance on 1987-02-24 under 510(k) number K864770. The device is classified under product code FFA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION TUBE?

SUCTION TUBE is a medical device that received FDA 510(k) clearance on 1987-02-24. The listed applicant is New England Surgical Instrument Corp.. The 510(k) number is K864770.

When did SUCTION TUBE receive FDA 510(k) clearance?

SUCTION TUBE received FDA 510(k) clearance on 1987-02-24, under 510(k) number K864770.

Who is the listed applicant for SUCTION TUBE?

The FDA 510(k) record lists New England Surgical Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION TUBE?

The FDA product code for SUCTION TUBE is FFA.

Related Clinical Trials

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.

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Other records listing New England Surgical Instrument 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.

K895337ELECTROSURGICAL COAGULATION SUCTION TUBEK895331ELECTROSURGICAL ELECTRODEK883963RANEY AND LEROY-RANEY SCALP CLIPK883396HANDSWITCHING MONOPOLAR PENCILK880863BIPOLAR MICRO COAGULATOR MODELS 25-1000 & 25-1200K880859SURGICAL BURS

View all 18 devices →

Related Devices (Code: FFA)

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.

K944290CATHETERS, BILIARY CATHETERS, UROLOGICALBoston Scientific CorpK833061C-FLEX PENROSE DRAINAGE TUBEConcept, 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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