FUTURA JUNIOR 300/310
K-Number: K943262 · 1994-09-29
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Device Summary
Frequently Asked Questions
What is the FUTURA JUNIOR 300/310?
FUTURA JUNIOR 300/310 is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Merivaara Instrumentarium Corp.. The 510(k) number is K943262.
When did FUTURA JUNIOR 300/310 receive FDA 510(k) clearance?
FUTURA JUNIOR 300/310 received FDA 510(k) clearance on 1994-09-29, under 510(k) number K943262.
Who is the listed applicant for FUTURA JUNIOR 300/310?
The FDA 510(k) record lists Merivaara Instrumentarium Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FUTURA JUNIOR 300/310?
The FDA product code for FUTURA JUNIOR 300/310 is FPO.
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 Merivaara Instrumentarium 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: FPO)
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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