FDA 510(k)

DW234 #29

K-Number: K941625 · 1994-06-22

Decision Date1994-06-22

Product CodeEJS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DW234 #29 is the device name listed in this FDA 510(k) record. The listed applicant is Rms Div.. It received FDA 510(k) clearance on 1994-06-22 under 510(k) number K941625. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DW234 #29?

DW234 #29 is a medical device that received FDA 510(k) clearance on 1994-06-22. The listed applicant is Rms Div.. The 510(k) number is K941625.

When did DW234 #29 receive FDA 510(k) clearance?

DW234 #29 received FDA 510(k) clearance on 1994-06-22, under 510(k) number K941625.

Who is the listed applicant for DW234 #29?

The FDA 510(k) record lists Rms Div. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DW234 #29?

The FDA product code for DW234 #29 is EJS.

Other records listing Rms Div. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K963367RMS K-WIRE K954438SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE K944848THE VIVACARE T.P.S. PROBE K944557DW250 #91 K902403ELITE R/F SPOT FILM DRIVE K902146SFD-035 SPOT FILM DEVICE

View all 10 devices →

Related Devices (Code: EJS)

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KG K022252STERNGOLD 1, MODEL 1127781Sterngold K022469ECO E4Wieland Dental + Technik GmbH & Co. KG K021367STERNGOLD 66, MODEL #1180230Sterngold K020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.