EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5%
K-Number: K850720 · 1985-03-22
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Device Summary
Frequently Asked Questions
What is the EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5%?
EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5% is a medical device that received FDA 510(k) clearance on 1985-03-22. The listed applicant is Rapid City Regional Hospital, Inc.. The 510(k) number is K850720.
When did EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5% receive FDA 510(k) clearance?
EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5% received FDA 510(k) clearance on 1985-03-22, under 510(k) number K850720.
Who is the listed applicant for EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5%?
The FDA 510(k) record lists Rapid City Regional Hospital, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5%?
The FDA product code for EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5% is JSI.
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 Rapid City Regional Hospital, 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: JSI)
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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