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FDA 510(k)

BYRON SUCTION TIPS

K-Number: K861878 · 1986-07-01

ApplicantByron Medical
Decision Date1986-07-01
Product Code
DecisionSubstantially Equivalent for Some Indications

Device Summary

BYRON SUCTION TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Byron Medical. It received FDA 510(k) clearance on 1986-07-01 under 510(k) number K861878. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the BYRON SUCTION TIPS?

BYRON SUCTION TIPS is a medical device that received FDA 510(k) clearance on 1986-07-01. The listed applicant is Byron Medical. The 510(k) number is K861878.

When did BYRON SUCTION TIPS receive FDA 510(k) clearance?

BYRON SUCTION TIPS received FDA 510(k) clearance on 1986-07-01, under 510(k) number K861878.

Who is the listed applicant for BYRON SUCTION TIPS?

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

Related Clinical Trials

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.

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Other records listing Byron Medical 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.

K040149PSI-TEC PERISTALTIC INFILTRATION PUMPK001803ACCELERATOR RECIPROCATING CANNULAK981215PSI-TEC LIPOSUCTION ASPIRATORK981172LIPOPLASTY/ LIPOSUCTION ASPIRATION AND TUMESCENT INFUSION CANNULAE AND NEEDLESK980738PSI-TEC SYRINGE INFUSION PUMP AND ACCESSORIES FOR GENERAL FLUID IRRIGAION/INFILTRATIONK980392PSI-TEC ASPIRATOR

View all 27 devices →

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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