MEDLINE OPEN END FINGER CONTROL MITT
K-Number: K963504 · 1996-10-29
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Device Summary
Frequently Asked Questions
What is the MEDLINE OPEN END FINGER CONTROL MITT?
MEDLINE OPEN END FINGER CONTROL MITT is a medical device that received FDA 510(k) clearance on 1996-10-29. The listed applicant is Medline. The 510(k) number is K963504.
When did MEDLINE OPEN END FINGER CONTROL MITT receive FDA 510(k) clearance?
MEDLINE OPEN END FINGER CONTROL MITT received FDA 510(k) clearance on 1996-10-29, under 510(k) number K963504.
Who is the listed applicant for MEDLINE OPEN END FINGER CONTROL MITT?
The FDA 510(k) record lists Medline as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDLINE OPEN END FINGER CONTROL MITT?
The FDA product code for MEDLINE OPEN END FINGER CONTROL MITT is FMQ.
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 Medline 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: FMQ)
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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