MINISPIROMETER SP-1
K-Number: K791422 · 1979-11-05
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Device Summary
Frequently Asked Questions
What is the MINISPIROMETER SP-1?
MINISPIROMETER SP-1 is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Renesco International, Inc.. The 510(k) number is K791422.
When did MINISPIROMETER SP-1 receive FDA 510(k) clearance?
MINISPIROMETER SP-1 received FDA 510(k) clearance on 1979-11-05, under 510(k) number K791422.
Who is the listed applicant for MINISPIROMETER SP-1?
The FDA 510(k) record lists Renesco International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINISPIROMETER SP-1?
The FDA product code for MINISPIROMETER SP-1 is BZG.
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 Renesco International, 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: BZG)
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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