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FDA 510(k)

PRO-SOFT DEHYDRANT

K-Number: K842863 · 1984-08-21

ApplicantAnatech, Ltd.
Decision Date1984-08-21
Product CodePPM
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

PRO-SOFT DEHYDRANT is the device name listed in this FDA 510(k) record. The listed applicant is Anatech, Ltd.. It received FDA 510(k) clearance on 1984-08-21 under 510(k) number K842863. The device is classified under product code PPM. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-SOFT DEHYDRANT?

PRO-SOFT DEHYDRANT is a medical device that received FDA 510(k) clearance on 1984-08-21. The listed applicant is Anatech, Ltd.. The 510(k) number is K842863.

When did PRO-SOFT DEHYDRANT receive FDA 510(k) clearance?

PRO-SOFT DEHYDRANT received FDA 510(k) clearance on 1984-08-21, under 510(k) number K842863.

Who is the listed applicant for PRO-SOFT DEHYDRANT?

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

What is the FDA product code for PRO-SOFT DEHYDRANT?

The FDA product code for PRO-SOFT DEHYDRANT is PPM.

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Other records listing Anatech, Ltd. 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.

K882874ZINC FORMALINK882873FIELDTEX HEMATOXYLINK882268ZINC FORMALIN CONCENTRATEK881282XYLENEK872663DRY-FORMK872498HARRIS HEMATOXYLIN

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Related Devices (Code: PPM)

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.

K871533TOMTEC GRAM STAINER DECOLORIZERRemel Co.K863550POTASSIUM HYDROXIDE 10% W/VReagent Laboratory, Inc.K861890100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2Richard-Allan Medical Ind., Inc.K850916SPRAYFIXSurgipath Medical Industries, Inc.K850737TRANSPORT CULTURE MEDIUMRoseville Medical LaboratoriesuK8508450.85% SALINEMicro Media Laboratories

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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