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FDA 510(k)

PERFUSOR SECURA SYRINGE PUMP

K-Number: K882107 · 1988-08-11

ApplicantBurron Medical, Inc.
Decision Date1988-08-11
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PERFUSOR SECURA SYRINGE PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical, Inc.. It received FDA 510(k) clearance on 1988-08-11 under 510(k) number K882107. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERFUSOR SECURA SYRINGE PUMP?

PERFUSOR SECURA SYRINGE PUMP is a medical device that received FDA 510(k) clearance on 1988-08-11. The listed applicant is Burron Medical, Inc.. The 510(k) number is K882107.

When did PERFUSOR SECURA SYRINGE PUMP receive FDA 510(k) clearance?

PERFUSOR SECURA SYRINGE PUMP received FDA 510(k) clearance on 1988-08-11, under 510(k) number K882107.

Who is the listed applicant for PERFUSOR SECURA SYRINGE PUMP?

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

What is the FDA product code for PERFUSOR SECURA SYRINGE PUMP?

The FDA product code for PERFUSOR SECURA SYRINGE PUMP is FRN.

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Other records listing Burron Medical, Inc. as applicant

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K902401CELSITE(TM) IMPLANTABLE DRUG DELIVERY SYSTEMK896422BURRON AMBULATORY DRUG DELIVERY SYSTEMK884235COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KITK895191ANTI-THROMBOGENIC COATING FOR CATHETERSK895192SPINOCAN(R) CONTINUOUS SPINAL TRAYK884183BURRON TEFLON-COATED GUIDEWIRE

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Related Devices (Code: FRN)

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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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