ASTECH HOME PEAK FLOW METER
K-Number: K915060 · 1992-09-11
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Device Summary
Frequently Asked Questions
What is the ASTECH HOME PEAK FLOW METER?
ASTECH HOME PEAK FLOW METER is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Biotrine Corp.. The 510(k) number is K915060.
When did ASTECH HOME PEAK FLOW METER receive FDA 510(k) clearance?
ASTECH HOME PEAK FLOW METER received FDA 510(k) clearance on 1992-09-11, under 510(k) number K915060.
Who is the listed applicant for ASTECH HOME PEAK FLOW METER?
The FDA 510(k) record lists Biotrine Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASTECH HOME PEAK FLOW METER?
The FDA product code for ASTECH HOME PEAK FLOW METER is BZH.
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 Biotrine 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: BZH)
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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