MONOBLOC BM SERIES
K-Number: K111573 · 2011-08-26
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Device Summary
Frequently Asked Questions
What is the MONOBLOC BM SERIES?
MONOBLOC BM SERIES is a medical device that received FDA 510(k) clearance on 2011-08-26. The listed applicant is Hass Corp.. The 510(k) number is K111573.
When did MONOBLOC BM SERIES receive FDA 510(k) clearance?
MONOBLOC BM SERIES received FDA 510(k) clearance on 2011-08-26, under 510(k) number K111573.
Who is the listed applicant for MONOBLOC BM SERIES?
The FDA 510(k) record lists Hass Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MONOBLOC BM SERIES?
The FDA product code for MONOBLOC BM SERIES is EIH.
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 Hass 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: EIH)
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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