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FDA 510(k)

BURRON MULTI-AD SYRINGE CAP

K-Number: K801311 · 1980-06-17

ApplicantBurron Medical Products, Inc.
Decision Date1980-06-17
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BURRON MULTI-AD SYRINGE CAP 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 1980-06-17 under 510(k) number K801311. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURRON MULTI-AD SYRINGE CAP?

BURRON MULTI-AD SYRINGE CAP is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K801311.

When did BURRON MULTI-AD SYRINGE CAP receive FDA 510(k) clearance?

BURRON MULTI-AD SYRINGE CAP received FDA 510(k) clearance on 1980-06-17, under 510(k) number K801311.

Who is the listed applicant for BURRON MULTI-AD SYRINGE CAP?

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 BURRON MULTI-AD SYRINGE CAP?

The FDA product code for BURRON MULTI-AD SYRINGE CAP is FMF.

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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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