TELEDYNE DENSCO DRY TIPS SALIVA ABSORB-
K-Number: K843539 · 1985-05-23
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Device Summary
Frequently Asked Questions
What is the TELEDYNE DENSCO DRY TIPS SALIVA ABSORB-?
TELEDYNE DENSCO DRY TIPS SALIVA ABSORB- is a medical device that received FDA 510(k) clearance on 1985-05-23. The listed applicant is Molnlycke A/S Hospital Products. The 510(k) number is K843539.
When did TELEDYNE DENSCO DRY TIPS SALIVA ABSORB- receive FDA 510(k) clearance?
TELEDYNE DENSCO DRY TIPS SALIVA ABSORB- received FDA 510(k) clearance on 1985-05-23, under 510(k) number K843539.
Who is the listed applicant for TELEDYNE DENSCO DRY TIPS SALIVA ABSORB-?
The FDA 510(k) record lists Molnlycke A/S Hospital Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TELEDYNE DENSCO DRY TIPS SALIVA ABSORB-?
The FDA product code for TELEDYNE DENSCO DRY TIPS SALIVA ABSORB- is EFN.
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.
Other records listing Molnlycke A/S Hospital Products 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.
Related Devices (Code: EFN)
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.
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