Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CAMPY BRUCELLA AGAR PLATE

K-Number: K834417 · 1984-01-17

Decision Date1984-01-17
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CAMPY BRUCELLA AGAR PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Otisville Biotech, Inc.. It received FDA 510(k) clearance on 1984-01-17 under 510(k) number K834417. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMPY BRUCELLA AGAR PLATE?

CAMPY BRUCELLA AGAR PLATE is a medical device that received FDA 510(k) clearance on 1984-01-17. The listed applicant is Otisville Biotech, Inc.. The 510(k) number is K834417.

When did CAMPY BRUCELLA AGAR PLATE receive FDA 510(k) clearance?

CAMPY BRUCELLA AGAR PLATE received FDA 510(k) clearance on 1984-01-17, under 510(k) number K834417.

Who is the listed applicant for CAMPY BRUCELLA 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 CAMPY BRUCELLA AGAR PLATE?

The FDA product code for CAMPY BRUCELLA AGAR PLATE is JSJ.

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.

View all 98 devices →

Related Devices (Code: JSJ)

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.

↑