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FDA 510(k)

CRAWFORD LACRIMAL INTUBATION SET

K-Number: K800089 · 1980-03-03

Decision Date1980-03-03
Product CodeHNL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CRAWFORD LACRIMAL INTUBATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1980-03-03 under 510(k) number K800089. The device is classified under product code HNL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRAWFORD LACRIMAL INTUBATION SET?

CRAWFORD LACRIMAL INTUBATION SET is a medical device that received FDA 510(k) clearance on 1980-03-03. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K800089.

When did CRAWFORD LACRIMAL INTUBATION SET receive FDA 510(k) clearance?

CRAWFORD LACRIMAL INTUBATION SET received FDA 510(k) clearance on 1980-03-03, under 510(k) number K800089.

Who is the listed applicant for CRAWFORD LACRIMAL INTUBATION SET?

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

What is the FDA product code for CRAWFORD LACRIMAL INTUBATION SET?

The FDA product code for CRAWFORD LACRIMAL INTUBATION SET is HNL.

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 Jedmed Instrument 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.

View all 91 devices →

Related Devices (Code: HNL)

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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