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FDA 510(k)

MODIFIED NEW YORK MEDIUM

K-Number: K831359 · 1983-05-18

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1983-05-18
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MODIFIED NEW YORK MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1983-05-18 under 510(k) number K831359. 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 MODIFIED NEW YORK MEDIUM?

MODIFIED NEW YORK MEDIUM is a medical device that received FDA 510(k) clearance on 1983-05-18. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K831359.

When did MODIFIED NEW YORK MEDIUM receive FDA 510(k) clearance?

MODIFIED NEW YORK MEDIUM received FDA 510(k) clearance on 1983-05-18, under 510(k) number K831359.

Who is the listed applicant for MODIFIED NEW YORK MEDIUM?

The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED NEW YORK MEDIUM?

The FDA product code for MODIFIED NEW YORK MEDIUM 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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