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FDA 510(k)

THE GRIPPER(TM) PORT-A-CATH NEEDLES

K-Number: K870866 · 1987-06-25

ApplicantPharmacia, Inc.
Decision Date1987-06-25
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE GRIPPER(TM) PORT-A-CATH NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1987-06-25 under 510(k) number K870866. 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 THE GRIPPER(TM) PORT-A-CATH NEEDLES?

THE GRIPPER(TM) PORT-A-CATH NEEDLES is a medical device that received FDA 510(k) clearance on 1987-06-25. The listed applicant is Pharmacia, Inc.. The 510(k) number is K870866.

When did THE GRIPPER(TM) PORT-A-CATH NEEDLES receive FDA 510(k) clearance?

THE GRIPPER(TM) PORT-A-CATH NEEDLES received FDA 510(k) clearance on 1987-06-25, under 510(k) number K870866.

Who is the listed applicant for THE GRIPPER(TM) PORT-A-CATH NEEDLES?

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

What is the FDA product code for THE GRIPPER(TM) PORT-A-CATH NEEDLES?

The FDA product code for THE GRIPPER(TM) PORT-A-CATH NEEDLES is FPA.

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Other records listing Pharmacia, 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.

K974350ALLERGAN IMMUNO CAP M4, M8, K70K972364UNICAP PHADIATOPK972068UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0K964152UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMHK962274UNICAP 100

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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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