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FDA 510(k)

PRE-DUCED CULTURE MEDIA

K-Number: K770650 · 1977-04-15

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1977-04-15
Product CodeJSL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PRE-DUCED CULTURE MEDIA 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 1977-04-15 under 510(k) number K770650. The device is classified under product code JSL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-DUCED CULTURE MEDIA?

PRE-DUCED CULTURE MEDIA is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K770650.

When did PRE-DUCED CULTURE MEDIA receive FDA 510(k) clearance?

PRE-DUCED CULTURE MEDIA received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770650.

Who is the listed applicant for PRE-DUCED CULTURE MEDIA?

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 PRE-DUCED CULTURE MEDIA?

The FDA product code for PRE-DUCED CULTURE MEDIA is JSL.

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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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