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FDA 510(k)

AUTOMATIC TRAY (ACT I & ACT II

K-Number: K820117 · 1982-02-18

Decision Date1982-02-18
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC TRAY (ACT I & ACT II is the device name listed in this FDA 510(k) record. The listed applicant is Burbury & Cutter Ind., Inc.. It received FDA 510(k) clearance on 1982-02-18 under 510(k) number K820117. The device is classified under product code KPX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC TRAY (ACT I & ACT II?

AUTOMATIC TRAY (ACT I & ACT II is a medical device that received FDA 510(k) clearance on 1982-02-18. The listed applicant is Burbury & Cutter Ind., Inc.. The 510(k) number is K820117.

When did AUTOMATIC TRAY (ACT I & ACT II receive FDA 510(k) clearance?

AUTOMATIC TRAY (ACT I & ACT II received FDA 510(k) clearance on 1982-02-18, under 510(k) number K820117.

Who is the listed applicant for AUTOMATIC TRAY (ACT I & ACT II?

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

What is the FDA product code for AUTOMATIC TRAY (ACT I & ACT II?

The FDA product code for AUTOMATIC TRAY (ACT I & ACT II is KPX.

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.

Related Devices (Code: KPX)

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.

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