Spatula for Pap Smear Collection

FDA 510(k) K893229 · Medical Device Inspection Co., Inc.

Substantially Equivalent

510(k) numberK893229

Submission

Device name
Spatula for Pap Smear Collection
Applicant
Medical Device Inspection Co., Inc.
Great Neck, NY, US
Received
April 28, 1989
Decision date
February 22, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HHT – Spatula, Cervical, Cytological
Device class
Class II (moderate risk)
Regulation
21 CFR 884.4530
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Spatula for Pap Smear Collection cleared by the FDA?

Spatula for Pap Smear Collection (K893229) received a 510(k) decision of Substantially Equivalent on February 22, 1990, 300 days after the submission was received.

What is the product code of K893229?

The FDA product code is HHT – Spatula, Cervical, Cytological, a Class II (moderate risk) device regulated under 21 CFR 884.4530.