45DEGREES SWIVEL ELBOW
K-Number: K811922 · 1981-07-23
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Device Summary
Frequently Asked Questions
What is the 45DEGREES SWIVEL ELBOW?
45DEGREES SWIVEL ELBOW is a medical device that received FDA 510(k) clearance on 1981-07-23. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K811922.
When did 45DEGREES SWIVEL ELBOW receive FDA 510(k) clearance?
45DEGREES SWIVEL ELBOW received FDA 510(k) clearance on 1981-07-23, under 510(k) number K811922.
Who is the listed applicant for 45DEGREES SWIVEL ELBOW?
The FDA 510(k) record lists Dhd Medical Products Div. Diemolding Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 45DEGREES SWIVEL ELBOW?
The FDA product code for 45DEGREES SWIVEL ELBOW is BZA.
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 Dhd Medical Products Div. Diemolding 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.
Related Devices (Code: BZA)
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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