STABILOR NF
K-Number: K821521 · 1982-06-09
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Device Summary
Frequently Asked Questions
What is the STABILOR NF?
STABILOR NF is a medical device that received FDA 510(k) clearance on 1982-06-09. The listed applicant is J. Aderer, Inc.. The 510(k) number is K821521.
When did STABILOR NF receive FDA 510(k) clearance?
STABILOR NF received FDA 510(k) clearance on 1982-06-09, under 510(k) number K821521.
Who is the listed applicant for STABILOR NF?
The FDA 510(k) record lists J. Aderer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STABILOR NF?
The FDA product code for STABILOR NF is EJT.
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 J. Aderer, 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: EJT)
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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