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FDA 510(k)

ORTHOPEDIC/NALEBUFF FINGER INSTRUMENTS

K-Number: K831426 · 1983-06-08

ApplicantNew England Surgical Instrument Corp.
Decision Date1983-06-08
Product Code
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC/NALEBUFF FINGER INSTRUMENTS 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 1983-06-08 under 510(k) number K831426. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPEDIC/NALEBUFF FINGER INSTRUMENTS?

ORTHOPEDIC/NALEBUFF FINGER INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is New England Surgical Instrument Corp.. The 510(k) number is K831426.

When did ORTHOPEDIC/NALEBUFF FINGER INSTRUMENTS receive FDA 510(k) clearance?

ORTHOPEDIC/NALEBUFF FINGER INSTRUMENTS received FDA 510(k) clearance on 1983-06-08, under 510(k) number K831426.

Who is the listed applicant for ORTHOPEDIC/NALEBUFF FINGER INSTRUMENTS?

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

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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.

K895331ELECTROSURGICAL ELECTRODEK895337ELECTROSURGICAL COAGULATION SUCTION TUBEK883963RANEY AND LEROY-RANEY SCALP CLIPK883396HANDSWITCHING MONOPOLAR PENCILK880863BIPOLAR MICRO COAGULATOR MODELS 25-1000 & 25-1200K880859SURGICAL BURS

View all 18 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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