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FDA 510(k)

PERMA-SET INFUSION SET

K-Number: K822603 · 1982-09-14

ApplicantCosmetic Sciences, Inc.
Decision Date1982-09-14
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PERMA-SET INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Cosmetic Sciences, Inc.. It received FDA 510(k) clearance on 1982-09-14 under 510(k) number K822603. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERMA-SET INFUSION SET?

PERMA-SET INFUSION SET is a medical device that received FDA 510(k) clearance on 1982-09-14. The listed applicant is Cosmetic Sciences, Inc.. The 510(k) number is K822603.

When did PERMA-SET INFUSION SET receive FDA 510(k) clearance?

PERMA-SET INFUSION SET received FDA 510(k) clearance on 1982-09-14, under 510(k) number K822603.

Who is the listed applicant for PERMA-SET INFUSION SET?

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

What is the FDA product code for PERMA-SET INFUSION SET?

The FDA product code for PERMA-SET INFUSION SET is LDR.

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Other records listing Cosmetic Sciences, Inc. 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.

K842756BUTTERFLY II PN INFUSION NEEDLEK833682PRIMARY PIGGYBACK INFUSION SET W/PERMK830568GUTTMAN INFUSION NEEDLE

Related Devices (Code: LDR)

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.

K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development CorporationK232316DEKA Infusion System, DEKA Administration SetDeka Research and DevelopmentK153760Volumetric Infusion ControllerDEKA Research & DevelopmentK963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.K971865ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3PAlexander Mfg. Co.

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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