Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DISPENS-O-DISC DIFFERENTIATION DISKS PYR

K-Number: K862570 · 1986-07-17

Decision Date1986-07-17
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DISPENS-O-DISC DIFFERENTIATION DISKS PYR is the device name listed in this FDA 510(k) record. The listed applicant is Difco Laboratories, Inc.. It received FDA 510(k) clearance on 1986-07-17 under 510(k) number K862570. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPENS-O-DISC DIFFERENTIATION DISKS PYR?

DISPENS-O-DISC DIFFERENTIATION DISKS PYR is a medical device that received FDA 510(k) clearance on 1986-07-17. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K862570.

When did DISPENS-O-DISC DIFFERENTIATION DISKS PYR receive FDA 510(k) clearance?

DISPENS-O-DISC DIFFERENTIATION DISKS PYR received FDA 510(k) clearance on 1986-07-17, under 510(k) number K862570.

Who is the listed applicant for DISPENS-O-DISC DIFFERENTIATION DISKS PYR?

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

What is the FDA product code for DISPENS-O-DISC DIFFERENTIATION DISKS PYR?

The FDA product code for DISPENS-O-DISC DIFFERENTIATION DISKS PYR is JTO.

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.

Other records listing Difco Laboratories, 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.

View all 121 devices →

Related Devices (Code: JTO)

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.

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.

↑