ISOLA SLOTTED CONNECT/ANGLED SLOTTED CONNECTOR
K-Number: K905826 · 1991-03-21
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Device Summary
Frequently Asked Questions
What is the ISOLA SLOTTED CONNECT/ANGLED SLOTTED CONNECTOR?
ISOLA SLOTTED CONNECT/ANGLED SLOTTED CONNECTOR is a medical device that received FDA 510(k) clearance on 1991-03-21. The listed applicant is Acromed Corp.. The 510(k) number is K905826.
When did ISOLA SLOTTED CONNECT/ANGLED SLOTTED CONNECTOR receive FDA 510(k) clearance?
ISOLA SLOTTED CONNECT/ANGLED SLOTTED CONNECTOR received FDA 510(k) clearance on 1991-03-21, under 510(k) number K905826.
Who is the listed applicant for ISOLA SLOTTED CONNECT/ANGLED SLOTTED CONNECTOR?
The FDA 510(k) record lists Acromed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ISOLA SLOTTED CONNECT/ANGLED SLOTTED CONNECTOR?
The FDA product code for ISOLA SLOTTED CONNECT/ANGLED SLOTTED CONNECTOR is KWP.
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 Acromed 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: KWP)
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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