House Dust; Hollister-Stier (H/S) Allergen Disc

FDA 510(k) K875110 · Incstar Corp.

Substantially Equivalent

510(k) numberK875110

Submission

Device name
House Dust; Hollister-Stier (H/S) Allergen Disc
Applicant
Incstar Corp.
Stillwater, MN, US
Received
December 14, 1987
Decision date
June 14, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DHB – System, Test, Radioallergosorbent (Rast) Immunological
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5750
Specialty
Immunology

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Questions and answers

When was House Dust; Hollister-Stier (H/S) Allergen Disc cleared by the FDA?

House Dust; Hollister-Stier (H/S) Allergen Disc (K875110) received a 510(k) decision of Substantially Equivalent on June 14, 1988, 183 days after the submission was received.

What is the product code of K875110?

The FDA product code is DHB – System, Test, Radioallergosorbent (Rast) Immunological, a Class II (moderate risk) device regulated under 21 CFR 866.5750.