NEONATE MASK FOR BABIES— 510(k) K840444

Name: FDA 510(k) clearance K840444
Creator: U.S. Food and Drug Administration
Published: 1984-03-16

Substantially Equivalent

Richards Medical Co., Inc.

FDA 510(k) clearance K840444 for NEONATE MASK FOR BABIES, Substantially Equivalent on 1984-03-16. Applicant: Richards Medical Co., Inc.. Device class: 1.

Clearance details

Applicant: Richards Medical Co., Inc.
Product code: Code HOY
Device class: Class 1
Regulation: 21 CFR 886.4750
Advisory panel: Ophthalmic
Date received: 1984-02-01
Decision date: 1984-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HOY

view all

K132042 — AMB101 SYSTEM, AMBLYZ, LCG SYSTEM, XPAND2014-04-28
K050856 — LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM2005-05-31
K971465 — NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS1997-06-04
K944700 — ARCTIC PREMIER SERIES1994-12-22
K944857 — GOGGLE SAFEGUARD1994-12-15

More clearances from Richards Medical Co., Inc.

view all

K896106 — ROGOZINSKI SPINAL SYSTEM, ADD'L COMPONENTS1990-06-25
K900628 — MODULAR HIP SYSTEM1990-05-09
K896580 — UNI-POLAR HEAD1990-02-15
K895241 — INTRAMEDULLARY HIP SCREW1990-01-04
K884824 — TRICON-M TOTAL KNEE SYSTEM1989-11-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.