STRAITH NASAL SPLINT
K-Number: K801072 · 1980-06-17
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Device Summary
Frequently Asked Questions
What is the STRAITH NASAL SPLINT?
STRAITH NASAL SPLINT is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Surgical Technology Laboratories, Inc.. The 510(k) number is K801072.
When did STRAITH NASAL SPLINT receive FDA 510(k) clearance?
STRAITH NASAL SPLINT received FDA 510(k) clearance on 1980-06-17, under 510(k) number K801072.
Who is the listed applicant for STRAITH NASAL SPLINT?
The FDA 510(k) record lists Surgical Technology Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRAITH NASAL SPLINT?
The FDA product code for STRAITH NASAL SPLINT is FYI.
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 Surgical Technology Laboratories, 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: FYI)
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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