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FDA 510(k)

PRE-REDUCED MEDIA

K-Number: K780533 · 1978-04-18

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1978-04-18
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PRE-REDUCED 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 1978-04-18 under 510(k) number K780533. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-REDUCED MEDIA?

PRE-REDUCED MEDIA is a medical device that received FDA 510(k) clearance on 1978-04-18. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K780533.

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

PRE-REDUCED MEDIA received FDA 510(k) clearance on 1978-04-18, under 510(k) number K780533.

Who is the listed applicant for PRE-REDUCED 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-REDUCED MEDIA?

The FDA product code for PRE-REDUCED MEDIA is JSF.

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Related Devices (Code: JSF)

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K880946NUTRIENT GELATIN - PRODUCT NUMBER T2860Lakewood Biochemical Co., Inc.K880126LAURYL TRYPTOSE BROTHHardy MediaK880119MOELLERS DECARBOXYLASE, ONITHINEHardy MediaK880120MOELLERS DECARBOXYLASE, LYSINEHardy MediaK880139ONPG TEST REAGENTHardy MediaK880113CYSTINE TRYPTIC MEDIUM W/LACTOSEHardy Media

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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