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FDA 510(k)

PATIENT CONTROLLED SYRINGE PUMP TYPE 3300

K-Number: K915270 · 1992-08-24

ApplicantGraseby Medical , Ltd.
Decision Date1992-08-24
Product CodeMEA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT CONTROLLED SYRINGE PUMP TYPE 3300 is the device name listed in this FDA 510(k) record. The listed applicant is Graseby Medical , Ltd.. It received FDA 510(k) clearance on 1992-08-24 under 510(k) number K915270. The device is classified under product code MEA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT CONTROLLED SYRINGE PUMP TYPE 3300?

PATIENT CONTROLLED SYRINGE PUMP TYPE 3300 is a medical device that received FDA 510(k) clearance on 1992-08-24. The listed applicant is Graseby Medical , Ltd.. The 510(k) number is K915270.

When did PATIENT CONTROLLED SYRINGE PUMP TYPE 3300 receive FDA 510(k) clearance?

PATIENT CONTROLLED SYRINGE PUMP TYPE 3300 received FDA 510(k) clearance on 1992-08-24, under 510(k) number K915270.

Who is the listed applicant for PATIENT CONTROLLED SYRINGE PUMP TYPE 3300?

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

What is the FDA product code for PATIENT CONTROLLED SYRINGE PUMP TYPE 3300?

The FDA product code for PATIENT CONTROLLED SYRINGE PUMP TYPE 3300 is MEA.

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Other records listing Graseby Medical , 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.

K9447219000 INFUSION PUMPK9313183400 INFUSION PUMPK9121933000 INFUSION PUMPK9121923100 INFUSION PUMP

Related Devices (Code: MEA)

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.

K162165ambIT PCA*PIB, ambIT PIB, ambIT PIB*PCA, ambIT PIEB, and ambIT Programmable Intermittent PumpSummit Medical Products, Inc.K170982CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion Pump, Model 2110; PharmGuard® Administrator Medication Safety Software; CADD® Administration Sets; Wireless Communication Module (CM)Smiths Medical Ads, Inc.K143612LifeCare PCA Infusion SystemHospira, Inc.K130394CADD -SOLIS AMBULATORY INFUSION PUMP, VERSION 3.0Smiths Medical Asd, Inc.K092313PERFUSOR SPACE INFUSION SYRINGE PUMP SYSTEMB.Braun Medical, Inc.K072144CADD -SOLIS AMBULATORY INFUSION PUMP AND CADD -SOLIS MEDICATION SAFETY SOFTWARE - ADMINISTRATORSmiths Medical MD, Inc.

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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