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FDA 510(k)

DORC CORNEAL PUNCH BLOCK

K-Number: K830335 · 1983-03-09

Decision Date1983-03-09
Product CodeHNJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DORC CORNEAL PUNCH BLOCK 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 1983-03-09 under 510(k) number K830335. The device is classified under product code HNJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DORC CORNEAL PUNCH BLOCK?

DORC CORNEAL PUNCH BLOCK is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K830335.

When did DORC CORNEAL PUNCH BLOCK receive FDA 510(k) clearance?

DORC CORNEAL PUNCH BLOCK received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830335.

Who is the listed applicant for DORC CORNEAL PUNCH BLOCK?

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 DORC CORNEAL PUNCH BLOCK?

The FDA product code for DORC CORNEAL PUNCH BLOCK is HNJ.

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: HNJ)

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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