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FDA 510(k)

KONTRON LITWAK-KOFFSKY OBTURATED CANNU

K-Number: K821316 · 1982-08-06

ApplicantKontron Instruments, Inc.
Decision Date1982-08-06
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KONTRON LITWAK-KOFFSKY OBTURATED CANNU is the device name listed in this FDA 510(k) record. The listed applicant is Kontron Instruments, Inc.. It received FDA 510(k) clearance on 1982-08-06 under 510(k) number K821316. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KONTRON LITWAK-KOFFSKY OBTURATED CANNU?

KONTRON LITWAK-KOFFSKY OBTURATED CANNU is a medical device that received FDA 510(k) clearance on 1982-08-06. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K821316.

When did KONTRON LITWAK-KOFFSKY OBTURATED CANNU receive FDA 510(k) clearance?

KONTRON LITWAK-KOFFSKY OBTURATED CANNU received FDA 510(k) clearance on 1982-08-06, under 510(k) number K821316.

Who is the listed applicant for KONTRON LITWAK-KOFFSKY OBTURATED CANNU?

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

What is the FDA product code for KONTRON LITWAK-KOFFSKY OBTURATED CANNU?

The FDA product code for KONTRON LITWAK-KOFFSKY OBTURATED CANNU is DWF.

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Other records listing Kontron Instruments, Inc. as applicant

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Related Devices (Code: DWF)

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.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, 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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