BROWNE MVI ETHYLENE OXIDE INDICATOR
K-Number: K991418 · 1999-06-10
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Device Summary
Frequently Asked Questions
What is the BROWNE MVI ETHYLENE OXIDE INDICATOR?
BROWNE MVI ETHYLENE OXIDE INDICATOR is a medical device that received FDA 510(k) clearance on 1999-06-10. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K991418.
When did BROWNE MVI ETHYLENE OXIDE INDICATOR receive FDA 510(k) clearance?
BROWNE MVI ETHYLENE OXIDE INDICATOR received FDA 510(k) clearance on 1999-06-10, under 510(k) number K991418.
Who is the listed applicant for BROWNE MVI ETHYLENE OXIDE INDICATOR?
The FDA 510(k) record lists Albert Browne , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BROWNE MVI ETHYLENE OXIDE INDICATOR?
The FDA product code for BROWNE MVI ETHYLENE OXIDE INDICATOR is JOJ.
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 Albert Browne , Ltd. 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: JOJ)
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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