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FDA 510(k)

STORZ ENT/OPHTHALMIC MAXI CHAIR

K-Number: K870112 · 1987-02-12

Decision Date1987-02-12
Product CodeHME
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STORZ ENT/OPHTHALMIC MAXI CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1987-02-12 under 510(k) number K870112. The device is classified under product code HME. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ ENT/OPHTHALMIC MAXI CHAIR?

STORZ ENT/OPHTHALMIC MAXI CHAIR is a medical device that received FDA 510(k) clearance on 1987-02-12. The listed applicant is Storz Instrument Co.. The 510(k) number is K870112.

When did STORZ ENT/OPHTHALMIC MAXI CHAIR receive FDA 510(k) clearance?

STORZ ENT/OPHTHALMIC MAXI CHAIR received FDA 510(k) clearance on 1987-02-12, under 510(k) number K870112.

Who is the listed applicant for STORZ ENT/OPHTHALMIC MAXI CHAIR?

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

What is the FDA product code for STORZ ENT/OPHTHALMIC MAXI CHAIR?

The FDA product code for STORZ ENT/OPHTHALMIC MAXI CHAIR is HME.

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 Storz 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 101 devices →

Related Devices (Code: HME)

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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