Disposable Dispense Manifold

by Dynatech Laboratories, Inc. 510(k)

Active United States

510(k) K823218

Regulatory status

as of 27 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK823218	Date16 Nov 1982Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 10 Oct 2026.

Specification

510(k)

510(k) Number: K823218
FDA Product Code: JTC

Device Class: Class I
Regulation: 21 CFR Part 866.2500
Advisory Committee: Microbiology
FDA Decision: SESE Substantially Equivalent

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