S 22 INSTRUMENT STAND
K-Number: K891584 · 1989-06-08
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Device Summary
Frequently Asked Questions
What is the S 22 INSTRUMENT STAND?
S 22 INSTRUMENT STAND is a medical device that received FDA 510(k) clearance on 1989-06-08. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K891584.
When did S 22 INSTRUMENT STAND receive FDA 510(k) clearance?
S 22 INSTRUMENT STAND received FDA 510(k) clearance on 1989-06-08, under 510(k) number K891584.
Who is the listed applicant for S 22 INSTRUMENT STAND?
The FDA 510(k) record lists Carl Zeiss, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S 22 INSTRUMENT STAND?
The FDA product code for S 22 INSTRUMENT STAND is HRM.
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 Carl Zeiss, Inc. 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: HRM)
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.
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