VAPOR-TECH SLED ELECTRODE
K-Number: K970717 · 1997-05-08
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Device Summary
Frequently Asked Questions
What is the VAPOR-TECH SLED ELECTRODE?
VAPOR-TECH SLED ELECTRODE is a medical device that received FDA 510(k) clearance on 1997-05-08. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K970717.
When did VAPOR-TECH SLED ELECTRODE receive FDA 510(k) clearance?
VAPOR-TECH SLED ELECTRODE received FDA 510(k) clearance on 1997-05-08, under 510(k) number K970717.
Who is the listed applicant for VAPOR-TECH SLED ELECTRODE?
The FDA 510(k) record lists Northgate Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VAPOR-TECH SLED ELECTRODE?
The FDA product code for VAPOR-TECH SLED ELECTRODE is FAS.
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 Northgate Technologies, 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: FAS)
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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