510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K844657Substantially Equivalent

Spectable Frame Magnifying Brillette

Pro Design Intl. AS, New York NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K844657 is the FDA 510(k) clearance record for SPECTABLE FRAME MAGNIFYING BRILLETTE, a class I device, cleared for Pro Design Intl. AS on under FDA product code HOJ (Screen, Tangent, Target). FDA records list 2 510(k) clearances for Pro Design Intl. AS. As of , FDA records show no recalls naming K844657.

Clearance record

Decision date
Received
(12 days to decision)
Product code
HOJ Screen, Tangent, Target
Regulation
21 CFR 886.1810
Device class
Class I
Review panel
Ophthalmic
Applicant
Pro Design Intl. AS 20 Waterside Plz., New York NY
Third party review
No

Clearances, product code HOJ

Trailing 12 months

FDA records hold no clearances under product code HOJ in the trailing twelve months.

FDA records show no clearances under product code HOJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HOJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260