NOVAMETRIX NAVAGRAPH MODEL 312 RECORDER
K-Number: K813351 · 1981-12-31
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Device Summary
Frequently Asked Questions
What is the NOVAMETRIX NAVAGRAPH MODEL 312 RECORDER?
NOVAMETRIX NAVAGRAPH MODEL 312 RECORDER is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K813351.
When did NOVAMETRIX NAVAGRAPH MODEL 312 RECORDER receive FDA 510(k) clearance?
NOVAMETRIX NAVAGRAPH MODEL 312 RECORDER received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813351.
Who is the listed applicant for NOVAMETRIX NAVAGRAPH MODEL 312 RECORDER?
The FDA 510(k) record lists Novametrix Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NOVAMETRIX NAVAGRAPH MODEL 312 RECORDER?
The FDA product code for NOVAMETRIX NAVAGRAPH MODEL 312 RECORDER is KLK.
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.
Other records listing Novametrix Medical Systems, Inc. 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.
Related Devices (Code: KLK)
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.
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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