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FDA 510(k)

STAPHYLOCOCCUS MEDIUM 1100

K-Number: K821426 · 1982-06-01

Decision Date1982-06-01
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

STAPHYLOCOCCUS MEDIUM 1100 is the device name listed in this FDA 510(k) record. The listed applicant is Interstate Media. It received FDA 510(k) clearance on 1982-06-01 under 510(k) number K821426. 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 STAPHYLOCOCCUS MEDIUM 1100?

STAPHYLOCOCCUS MEDIUM 1100 is a medical device that received FDA 510(k) clearance on 1982-06-01. The listed applicant is Interstate Media. The 510(k) number is K821426.

When did STAPHYLOCOCCUS MEDIUM 1100 receive FDA 510(k) clearance?

STAPHYLOCOCCUS MEDIUM 1100 received FDA 510(k) clearance on 1982-06-01, under 510(k) number K821426.

Who is the listed applicant for STAPHYLOCOCCUS MEDIUM 1100?

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

What is the FDA product code for STAPHYLOCOCCUS MEDIUM 1100?

The FDA product code for STAPHYLOCOCCUS MEDIUM 1100 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 Interstate Media 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 15 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.

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