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FDA 510(k)

SPINOCAN SPINAL NEEDLE

K-Number: K820047 · 1982-01-25

ApplicantBurron Medical Products, Inc.
Decision Date1982-01-25
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPINOCAN SPINAL NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1982-01-25 under 510(k) number K820047. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINOCAN SPINAL NEEDLE?

SPINOCAN SPINAL NEEDLE is a medical device that received FDA 510(k) clearance on 1982-01-25. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K820047.

When did SPINOCAN SPINAL NEEDLE receive FDA 510(k) clearance?

SPINOCAN SPINAL NEEDLE received FDA 510(k) clearance on 1982-01-25, under 510(k) number K820047.

Who is the listed applicant for SPINOCAN SPINAL NEEDLE?

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

What is the FDA product code for SPINOCAN SPINAL NEEDLE?

The FDA product code for SPINOCAN SPINAL NEEDLE is BSP.

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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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