510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K003775Substantially Equivalent

Portable Breast Compression Device

Pem Technologies, Rockville MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K003775 is the FDA 510(k) clearance record for PORTABLE BREAST COMPRESSION DEVICE, a class I device, cleared for Pem Technologies on under FDA product code IYX (Camera, Scintillation (Gamma)). FDA records list 2 510(k) clearances for Pem Technologies, from to . As of , FDA records show no recalls naming K003775.

Clearance record

Decision date
Received
(37 days to decision)
Product code
IYX Camera, Scintillation (Gamma)
Regulation
21 CFR 892.1100
Device class
Class I
Review panel
Radiology
Applicant
Pem Technologies 12300 Twinbrook Pkwy., Suite 625, Rockville MD
510(k) summary
Summary
Third party review
No

Clearances, product code IYX

Trailing 12 months

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

FDA records show no clearances under product code IYX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IYX, 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