ClearanceBrief
Company ยท US

Apothecary Products, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 2014. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
2recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KCMDropper, Ent2
EWDProtector, Hearing (Insert)1
LRXCase, Contact Lens1
LXQCup, Eye1
LYYLatex Patient Examination Glove1
MVVDevice, Acupressure1
NXBDispenser, Solid Medication1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 9, 2014K140409FLENTS PLASTIC EYE WASH CUP
Apothecary Products, Inc.
LXQ
Jul 14, 2011K111856SOFT GRIP CONTACT LENS CASE, DELUXE CONTACT LENS CASE, ECONO-MATE CONTACT LENS CASE
Apothecary Products, Inc.
LRX
Nov 26, 2004K041766EZY-TRAVEL WRISTBAND
Apothecary Products, Inc.
MVV
Jun 25, 2002K020296ADULT SILICONE EAR PLUGS, MODELS # 68053, 68057
Apothecary Products, Inc.
EWD
May 12, 1989K892242PATIENT EXAMINATION GLOVES (LATEX)
Apothecary Products, Inc.
LYY
Feb 4, 1984K833311NITROGLYCERINE CONTAINER
Apothecary Products, Inc.
NXB

Latest recalls

DateFirm and productCodeLinked 510(k)
Jun 9, 2023Apothecary Products, LLC
Medicine Dropper, Product Code K508
Open, Classified
KCMNone listed
Jun 9, 2023Apothecary Products, LLC
Eye and Ear Dropper, Product Code 67082
Open, Classified
KCMNone listed
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