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FDA 510(k)

CHEMO-SPIKE RECONSTITUTION DEVICE

K-Number: K895290 · 1989-12-27

ApplicantThe Medi-Dose Group
Decision Date1989-12-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHEMO-SPIKE RECONSTITUTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is The Medi-Dose Group. It received FDA 510(k) clearance on 1989-12-27 under 510(k) number K895290. 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 CHEMO-SPIKE RECONSTITUTION DEVICE?

CHEMO-SPIKE RECONSTITUTION DEVICE is a medical device that received FDA 510(k) clearance on 1989-12-27. The listed applicant is The Medi-Dose Group. The 510(k) number is K895290.

When did CHEMO-SPIKE RECONSTITUTION DEVICE receive FDA 510(k) clearance?

CHEMO-SPIKE RECONSTITUTION DEVICE received FDA 510(k) clearance on 1989-12-27, under 510(k) number K895290.

Who is the listed applicant for CHEMO-SPIKE RECONSTITUTION DEVICE?

The FDA 510(k) record lists The Medi-Dose Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHEMO-SPIKE RECONSTITUTION DEVICE?

The FDA product code for CHEMO-SPIKE RECONSTITUTION DEVICE is FPA.

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Other records listing The Medi-Dose Group 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.

K952242TRANSFEER SPIKE IIK9426251.2 MICRON AIR ELIMINATING FILTERK900651TS-1800 MEDICATION TRANSFER SPIKEK895291IV DISPESNSING SPIKEK896291INJECTION PORT II --- FOR INTERMITTENT INJECTIONK895419DISPOSABLE DISC FILTER

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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

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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