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FDA 510(k)

SF REFEEDING MEDIA

K-Number: K831685 · 1983-07-06

ApplicantViromed Laboratories, Inc.
Decision Date1983-07-06
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SF REFEEDING MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Viromed Laboratories, Inc.. It received FDA 510(k) clearance on 1983-07-06 under 510(k) number K831685. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SF REFEEDING MEDIA?

SF REFEEDING MEDIA is a medical device that received FDA 510(k) clearance on 1983-07-06. The listed applicant is Viromed Laboratories, Inc.. The 510(k) number is K831685.

When did SF REFEEDING MEDIA receive FDA 510(k) clearance?

SF REFEEDING MEDIA received FDA 510(k) clearance on 1983-07-06, under 510(k) number K831685.

Who is the listed applicant for SF REFEEDING MEDIA?

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

What is the FDA product code for SF REFEEDING MEDIA?

The FDA product code for SF REFEEDING MEDIA is KIT.

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Other records listing Viromed Laboratories, Inc. as applicant

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Related Devices (Code: KIT)

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.

K892938AMNIO-GROW TMInovar Biologicals, Inc.K890700MELANOCYTE GROWTH MEDIUM (MGM)Clonetics Corp.K890701ENDOTHELIAL GROWTH MEDIUM (EGM)Clonetics Corp.K890482ABC, ABC-1X, ABC(TM)Cell Ent., Inc.K884654ALPHACALF SERUMHyclone Laboratories, Inc.K884572RPMI-1640 HYBRI-MAX, PROD. NO. R5382Sigma Chemical Co.

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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