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FDA 510(k)

NAMIC DUAL BACKCHECK VALVE

K-Number: K884408 · 1989-01-12

ApplicantNorth American Instrument Corp.
Decision Date1989-01-12
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NAMIC DUAL BACKCHECK VALVE is the device name listed in this FDA 510(k) record. The listed applicant is North American Instrument Corp.. It received FDA 510(k) clearance on 1989-01-12 under 510(k) number K884408. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAMIC DUAL BACKCHECK VALVE?

NAMIC DUAL BACKCHECK VALVE is a medical device that received FDA 510(k) clearance on 1989-01-12. The listed applicant is North American Instrument Corp.. The 510(k) number is K884408.

When did NAMIC DUAL BACKCHECK VALVE receive FDA 510(k) clearance?

NAMIC DUAL BACKCHECK VALVE received FDA 510(k) clearance on 1989-01-12, under 510(k) number K884408.

Who is the listed applicant for NAMIC DUAL BACKCHECK VALVE?

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

What is the FDA product code for NAMIC DUAL BACKCHECK VALVE?

The FDA product code for NAMIC DUAL BACKCHECK VALVE is DTL.

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Other records listing North American 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.

K960801SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)K955554HEMO-VALVEK960310EPIC INTRODUCER SHEATHK922552MORSE(R) ANGIOGRAPHIC CATHETERSK915078MORSE HEMOSTATIC CATHETER INTRODUCER SETK905208MORSE ANESTHESIA

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Related Devices (Code: DTL)

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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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