S S AGAR PLATE
K-Number: K834423 · 1984-10-23
Advertisement
Device Summary
Frequently Asked Questions
What is the S S AGAR PLATE?
S S AGAR PLATE is a medical device that received FDA 510(k) clearance on 1984-10-23. The listed applicant is Otisville Biotech, Inc.. The 510(k) number is K834423.
When did S S AGAR PLATE receive FDA 510(k) clearance?
S S AGAR PLATE received FDA 510(k) clearance on 1984-10-23, under 510(k) number K834423.
Who is the listed applicant for S S AGAR PLATE?
The FDA 510(k) record lists Otisville Biotech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S S AGAR PLATE?
The FDA product code for S S AGAR PLATE 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 Otisville Biotech, 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.
Advertisement