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FDA 510(k)

SAFETY-MULTIFLY

K-Number: K032150 · 2003-09-12

ApplicantSarstedt, Inc.
Decision Date2003-09-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFETY-MULTIFLY is the device name listed in this FDA 510(k) record. The listed applicant is Sarstedt, Inc.. It received FDA 510(k) clearance on 2003-09-12 under 510(k) number K032150. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFETY-MULTIFLY?

SAFETY-MULTIFLY is a medical device that received FDA 510(k) clearance on 2003-09-12. The listed applicant is Sarstedt, Inc.. The 510(k) number is K032150.

When did SAFETY-MULTIFLY receive FDA 510(k) clearance?

SAFETY-MULTIFLY received FDA 510(k) clearance on 2003-09-12, under 510(k) number K032150.

Who is the listed applicant for SAFETY-MULTIFLY?

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

What is the FDA product code for SAFETY-MULTIFLY?

The FDA product code for SAFETY-MULTIFLY is FPA.

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.

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Other records listing Sarstedt, 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.

K051019SAFETY NEEDLEK031359S-MONOVETTE EDTA K2-GELK024237URINE MONOVETTE BORIC ACIDK003382SARSTEDT NEEDLE PROTECTORK913622HEMOPLUS

Related Devices (Code: FPA)

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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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