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FDA 510(k)

TELEDYNE DENSCO DRY TIPS SALIVA ABSORB-

K-Number: K843539 · 1985-05-23

Decision Date1985-05-23
Product CodeEFN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TELEDYNE DENSCO DRY TIPS SALIVA ABSORB- is the device name listed in this FDA 510(k) record. The listed applicant is Molnlycke A/S Hospital Products. It received FDA 510(k) clearance on 1985-05-23 under 510(k) number K843539. The device is classified under product code EFN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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

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