MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB
K-Number: K870073 · 1987-02-20
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Device Summary
Frequently Asked Questions
What is the MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB?
MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Clinical Connections, Inc.. The 510(k) number is K870073.
When did MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB receive FDA 510(k) clearance?
MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870073.
Who is the listed applicant for MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB?
The FDA 510(k) record lists Clinical Connections, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB?
The FDA product code for MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB is DTL.
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 Clinical Connections, 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: DTL)
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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