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FDA 510(k)

FENZL RETICLE

K-Number: K801733 · 1980-09-16

ApplicantRobert E. Fenzl, M.D.
Decision Date1980-09-16
Product CodeHOI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FENZL RETICLE is the device name listed in this FDA 510(k) record. The listed applicant is Robert E. Fenzl, M.D.. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K801733. The device is classified under product code HOI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FENZL RETICLE?

FENZL RETICLE is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Robert E. Fenzl, M.D.. The 510(k) number is K801733.

When did FENZL RETICLE receive FDA 510(k) clearance?

FENZL RETICLE received FDA 510(k) clearance on 1980-09-16, under 510(k) number K801733.

Who is the listed applicant for FENZL RETICLE?

The FDA 510(k) record lists Robert E. Fenzl, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FENZL RETICLE?

The FDA product code for FENZL RETICLE is HOI.

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Related Devices (Code: HOI)

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

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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