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FDA 510(k)

LARYNGOSCOPE ATTACHMENT PH2000

K-Number: K831255 · 1983-09-12

Decision Date1983-09-12
Product CodeEQN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LARYNGOSCOPE ATTACHMENT PH2000 is the device name listed in this FDA 510(k) record. The listed applicant is Eder Instrument Co, Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K831255. The device is classified under product code EQN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LARYNGOSCOPE ATTACHMENT PH2000?

LARYNGOSCOPE ATTACHMENT PH2000 is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Eder Instrument Co, Inc.. The 510(k) number is K831255.

When did LARYNGOSCOPE ATTACHMENT PH2000 receive FDA 510(k) clearance?

LARYNGOSCOPE ATTACHMENT PH2000 received FDA 510(k) clearance on 1983-09-12, under 510(k) number K831255.

Who is the listed applicant for LARYNGOSCOPE ATTACHMENT PH2000?

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

What is the FDA product code for LARYNGOSCOPE ATTACHMENT PH2000?

The FDA product code for LARYNGOSCOPE ATTACHMENT PH2000 is EQN.

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 Eder Instrument Co, 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 10 devices →

Related Devices (Code: EQN)

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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