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)

XYLOSE LYSINE DEOXYCHOLATE AGAR

K-Number: K811604 · 1981-06-25

Decision Date1981-06-25
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

XYLOSE LYSINE DEOXYCHOLATE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Micro Media Laboratories. It received FDA 510(k) clearance on 1981-06-25 under 510(k) number K811604. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XYLOSE LYSINE DEOXYCHOLATE AGAR?

XYLOSE LYSINE DEOXYCHOLATE AGAR is a medical device that received FDA 510(k) clearance on 1981-06-25. The listed applicant is Micro Media Laboratories. The 510(k) number is K811604.

When did XYLOSE LYSINE DEOXYCHOLATE AGAR receive FDA 510(k) clearance?

XYLOSE LYSINE DEOXYCHOLATE AGAR received FDA 510(k) clearance on 1981-06-25, under 510(k) number K811604.

Who is the listed applicant for XYLOSE LYSINE DEOXYCHOLATE AGAR?

The FDA 510(k) record lists Micro Media Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XYLOSE LYSINE DEOXYCHOLATE AGAR?

The FDA product code for XYLOSE LYSINE DEOXYCHOLATE AGAR 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 Micro Media Laboratories 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 52 devices →

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.

↑