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FDA 510(k)

0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX

K-Number: K920795 · 1992-07-13

ApplicantOptical Radiation Corp.
Decision Date1992-07-13
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX is the device name listed in this FDA 510(k) record. The listed applicant is Optical Radiation Corp.. It received FDA 510(k) clearance on 1992-07-13 under 510(k) number K920795. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX?

0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX is a medical device that received FDA 510(k) clearance on 1992-07-13. The listed applicant is Optical Radiation Corp.. The 510(k) number is K920795.

When did 0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX receive FDA 510(k) clearance?

0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX received FDA 510(k) clearance on 1992-07-13, under 510(k) number K920795.

Who is the listed applicant for 0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX?

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

What is the FDA product code for 0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX?

The FDA product code for 0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX is HQG.

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Other records listing Optical Radiation Corp. 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.

K863200COMPUTON(R)K853668ORC ORACLE

Related Devices (Code: HQG)

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.

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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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