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FDA 510(k)

ALSEVER'S SOLUTION (MODIFIED)

K-Number: K810783 · 1981-05-13

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

Device Summary

ALSEVER'S SOLUTION (MODIFIED) 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 K810783. 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 ALSEVER'S SOLUTION (MODIFIED)?

ALSEVER'S SOLUTION (MODIFIED) 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 K810783.

When did ALSEVER'S SOLUTION (MODIFIED) receive FDA 510(k) clearance?

ALSEVER'S SOLUTION (MODIFIED) received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810783.

Who is the listed applicant for ALSEVER'S SOLUTION (MODIFIED)?

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 ALSEVER'S SOLUTION (MODIFIED)?

The FDA product code for ALSEVER'S SOLUTION (MODIFIED) 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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