STORZ ENT/OPHTHALMIC MAXI CHAIR
K-Number: K870112 · 1987-02-12
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement