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FDA 510(k)

ANALYZER, PROGRAMMABLE DISCRETE (PDA)

K-Number: K760642 · 1976-12-09

Decision Date1976-12-09
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANALYZER, PROGRAMMABLE DISCRETE (PDA) is the device name listed in this FDA 510(k) record. The listed applicant is Anatronics Corp.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K760642. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYZER, PROGRAMMABLE DISCRETE (PDA)?

ANALYZER, PROGRAMMABLE DISCRETE (PDA) is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Anatronics Corp.. The 510(k) number is K760642.

When did ANALYZER, PROGRAMMABLE DISCRETE (PDA) receive FDA 510(k) clearance?

ANALYZER, PROGRAMMABLE DISCRETE (PDA) received FDA 510(k) clearance on 1976-12-09, under 510(k) number K760642.

Who is the listed applicant for ANALYZER, PROGRAMMABLE DISCRETE (PDA)?

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

What is the FDA product code for ANALYZER, PROGRAMMABLE DISCRETE (PDA)?

The FDA product code for ANALYZER, PROGRAMMABLE DISCRETE (PDA) is JJE.

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: JJE)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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