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FDA 510(k)

DAVRON PROF. SCRUB BRUSH-DRY/STERILE

K-Number: K831488 · 1983-06-08

ApplicantMinnetonka, Inc.
Decision Date1983-06-08
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DAVRON PROF. SCRUB BRUSH-DRY/STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Minnetonka, Inc.. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K831488. The device is classified under product code GEC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVRON PROF. SCRUB BRUSH-DRY/STERILE?

DAVRON PROF. SCRUB BRUSH-DRY/STERILE is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Minnetonka, Inc.. The 510(k) number is K831488.

When did DAVRON PROF. SCRUB BRUSH-DRY/STERILE receive FDA 510(k) clearance?

DAVRON PROF. SCRUB BRUSH-DRY/STERILE received FDA 510(k) clearance on 1983-06-08, under 510(k) number K831488.

Who is the listed applicant for DAVRON PROF. SCRUB BRUSH-DRY/STERILE?

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

What is the FDA product code for DAVRON PROF. SCRUB BRUSH-DRY/STERILE?

The FDA product code for DAVRON PROF. SCRUB BRUSH-DRY/STERILE is GEC.

Related Clinical Trials

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Other records listing Minnetonka, Inc. 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.

K883566MEDICATED COVERING COATED W/.5% HYDRO ADHESIVE GELK883619MEDICATED COVERING COATED W/1.0% HYDRO ADHES. GELK860843CHECK-UP PLAQUE FIGHTING GUM

Related Devices (Code: GEC)

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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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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