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FDA 510(k)

HUMAN BLOOD IN ALSEVER'S

K-Number: K811225 · 1981-06-12

ApplicantDutchland Laboratories, Inc.
Decision Date1981-06-12
Product CodeJSK
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HUMAN BLOOD IN ALSEVER'S 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 1981-06-12 under 510(k) number K811225. The device is classified under product code JSK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMAN BLOOD IN ALSEVER'S?

HUMAN BLOOD IN ALSEVER'S is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K811225.

When did HUMAN BLOOD IN ALSEVER'S receive FDA 510(k) clearance?

HUMAN BLOOD IN ALSEVER'S received FDA 510(k) clearance on 1981-06-12, under 510(k) number K811225.

Who is the listed applicant for HUMAN BLOOD IN ALSEVER'S?

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 HUMAN BLOOD IN ALSEVER'S?

The FDA product code for HUMAN BLOOD IN ALSEVER'S is JSK.

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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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