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FDA 510(k)

FLEXIGRAM AUTO LOADER SYSTEM

K-Number: K811525 · 1981-06-18

Decision Date1981-06-18
Product CodeJJG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FLEXIGRAM AUTO LOADER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Nucleonics Laboratories, Inc.. It received FDA 510(k) clearance on 1981-06-18 under 510(k) number K811525. The device is classified under product code JJG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIGRAM AUTO LOADER SYSTEM?

FLEXIGRAM AUTO LOADER SYSTEM is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Electro-Nucleonics Laboratories, Inc.. The 510(k) number is K811525.

When did FLEXIGRAM AUTO LOADER SYSTEM receive FDA 510(k) clearance?

FLEXIGRAM AUTO LOADER SYSTEM received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811525.

Who is the listed applicant for FLEXIGRAM AUTO LOADER SYSTEM?

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

What is the FDA product code for FLEXIGRAM AUTO LOADER SYSTEM?

The FDA product code for FLEXIGRAM AUTO LOADER SYSTEM is JJG.

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 Electro-Nucleonics 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 41 devices →

Related Devices (Code: JJG)

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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