MED. SUPPORT STOCKING-VENOFIT LASTOFLEX
K-Number: K842708 · 1984-10-09
Advertisement
Device Summary
Frequently Asked Questions
What is the MED. SUPPORT STOCKING-VENOFIT LASTOFLEX?
MED. SUPPORT STOCKING-VENOFIT LASTOFLEX is a medical device that received FDA 510(k) clearance on 1984-10-09. The listed applicant is Kundt + Co. AG. The 510(k) number is K842708.
When did MED. SUPPORT STOCKING-VENOFIT LASTOFLEX receive FDA 510(k) clearance?
MED. SUPPORT STOCKING-VENOFIT LASTOFLEX received FDA 510(k) clearance on 1984-10-09, under 510(k) number K842708.
Who is the listed applicant for MED. SUPPORT STOCKING-VENOFIT LASTOFLEX?
The FDA 510(k) record lists Kundt + Co. AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MED. SUPPORT STOCKING-VENOFIT LASTOFLEX?
The FDA product code for MED. SUPPORT STOCKING-VENOFIT LASTOFLEX is DWL.
Related Clinical Trials
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.
Related Devices (Code: DWL)
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.
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.
Advertisement