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FDA 510(k)

WATER-TISSUE CULTURE GRADE

K-Number: K810774 · 1981-05-13

ApplicantDutchland Laboratories, Inc.
Decision Date1981-05-13
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

WATER-TISSUE CULTURE GRADE is the device name listed in this FDA 510(k) record. The listed applicant is Dutchland Laboratories, Inc.. It received FDA 510(k) clearance on 1981-05-13 under 510(k) number K810774. 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 WATER-TISSUE CULTURE GRADE?

WATER-TISSUE CULTURE GRADE is a medical device that received FDA 510(k) clearance on 1981-05-13. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K810774.

When did WATER-TISSUE CULTURE GRADE receive FDA 510(k) clearance?

WATER-TISSUE CULTURE GRADE received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810774.

Who is the listed applicant for WATER-TISSUE CULTURE GRADE?

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

What is the FDA product code for WATER-TISSUE CULTURE GRADE?

The FDA product code for WATER-TISSUE CULTURE GRADE is KIT.

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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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