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FDA 510(k)

ASK-300

K-Number: K882977 · 1989-01-05

ApplicantMedical Repackers Co.
Decision Date1989-01-05
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ASK-300 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Repackers Co.. It received FDA 510(k) clearance on 1989-01-05 under 510(k) number K882977. The device is classified under product code DQR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASK-300?

ASK-300 is a medical device that received FDA 510(k) clearance on 1989-01-05. The listed applicant is Medical Repackers Co.. The 510(k) number is K882977.

When did ASK-300 receive FDA 510(k) clearance?

ASK-300 received FDA 510(k) clearance on 1989-01-05, under 510(k) number K882977.

Who is the listed applicant for ASK-300?

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

What is the FDA product code for ASK-300?

The FDA product code for ASK-300 is DQR.

Other records listing Medical Repackers Co. 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.

K890575ACCUTHERM PTS-200K881313IQK-200K881429YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH.K874674AIK-100 ANESTHESIA INDUCTION KIT/TRAY

Related Devices (Code: DQR)

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.

K131446INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLESIntegra LifeSciences CorporationK07355918 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA IIEdwards Lifesciences Research MedicalK051655ANGIODYNAMICS, INC., MICRO ACCESS KITSAngioDynamics, Inc.K030398CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221Cardiacassist, Inc.K960098RMI INTERNAL MAMMARY ARTERY CANNULAResearch Medical, Inc.K902674DATASCOPE ARTERIAL CANNULA W/ACCESS PORTDatascope Corp.

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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