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FDA 510(k)

CUSTOM PROCEDURAL TRAY PROCEDURAL KIT

K-Number: K853759 · 1985-11-17

ApplicantCharles Atkins & Co.
Decision Date1985-11-17
Product Code
DecisionUnknown

Device Summary

CUSTOM PROCEDURAL TRAY PROCEDURAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Charles Atkins & Co.. It received FDA 510(k) clearance on 1985-11-17 under 510(k) number K853759. FDA Decision: Unknown.

Frequently Asked Questions

What is the CUSTOM PROCEDURAL TRAY PROCEDURAL KIT?

CUSTOM PROCEDURAL TRAY PROCEDURAL KIT is a medical device that received FDA 510(k) clearance on 1985-11-17. The listed applicant is Charles Atkins & Co.. The 510(k) number is K853759.

When did CUSTOM PROCEDURAL TRAY PROCEDURAL KIT receive FDA 510(k) clearance?

CUSTOM PROCEDURAL TRAY PROCEDURAL KIT received FDA 510(k) clearance on 1985-11-17, under 510(k) number K853759.

Who is the listed applicant for CUSTOM PROCEDURAL TRAY PROCEDURAL KIT?

The FDA 510(k) record lists Charles Atkins & Co. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Charles Atkins & Co. 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.

K854613SURGICAL DRAPES, OPHTHALMIN

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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