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FDA 510(k)

MARTIN LEWIS AGAR CSI 3169

K-Number: K791447 · 1979-09-17

ApplicantClinical Sciences, Inc.
Decision Date1979-09-17
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MARTIN LEWIS AGAR CSI 3169 is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Sciences, Inc.. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791447. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN LEWIS AGAR CSI 3169?

MARTIN LEWIS AGAR CSI 3169 is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Clinical Sciences, Inc.. The 510(k) number is K791447.

When did MARTIN LEWIS AGAR CSI 3169 receive FDA 510(k) clearance?

MARTIN LEWIS AGAR CSI 3169 received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791447.

Who is the listed applicant for MARTIN LEWIS AGAR CSI 3169?

The FDA 510(k) record lists Clinical Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARTIN LEWIS AGAR CSI 3169?

The FDA product code for MARTIN LEWIS AGAR CSI 3169 is JTY.

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Related Devices (Code: JTY)

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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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