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FDA 510(k)

ACCELERATOR RECIPROCATING CANNULA

K-Number: K001803 · 2000-08-04

ApplicantByron Medical
Decision Date2000-08-04
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACCELERATOR RECIPROCATING CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Byron Medical. It received FDA 510(k) clearance on 2000-08-04 under 510(k) number K001803. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCELERATOR RECIPROCATING CANNULA?

ACCELERATOR RECIPROCATING CANNULA is a medical device that received FDA 510(k) clearance on 2000-08-04. The listed applicant is Byron Medical. The 510(k) number is K001803.

When did ACCELERATOR RECIPROCATING CANNULA receive FDA 510(k) clearance?

ACCELERATOR RECIPROCATING CANNULA received FDA 510(k) clearance on 2000-08-04, under 510(k) number K001803.

Who is the listed applicant for ACCELERATOR RECIPROCATING CANNULA?

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

What is the FDA product code for ACCELERATOR RECIPROCATING CANNULA?

The FDA product code for ACCELERATOR RECIPROCATING CANNULA is QPB.

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Other records listing Byron Medical as applicant

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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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