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FDA 510(k)

S 21 INSTRUMENT STAND

K-Number: K883578 · 1988-09-13

ApplicantCarl Zeiss, Inc.
Decision Date1988-09-13
Product CodeFSH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

S 21 INSTRUMENT STAND is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss, Inc.. It received FDA 510(k) clearance on 1988-09-13 under 510(k) number K883578. The device is classified under product code FSH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S 21 INSTRUMENT STAND?

S 21 INSTRUMENT STAND is a medical device that received FDA 510(k) clearance on 1988-09-13. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K883578.

When did S 21 INSTRUMENT STAND receive FDA 510(k) clearance?

S 21 INSTRUMENT STAND received FDA 510(k) clearance on 1988-09-13, under 510(k) number K883578.

Who is the listed applicant for S 21 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 21 INSTRUMENT STAND?

The FDA product code for S 21 INSTRUMENT STAND is FSH.

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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.

K013402VISULAS 532SK003885VISULAS YAG IIK993357IOLMASTERK983868OPMI TWINER SURGICAL MICROSCOPEK965139SURGICAL MICROSCOPE NAVIGATOR (SMN) SYSTEM/SURGICAL TOOL NAVIGATOR (STN) SYSTEMK961380CPC PROBE

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Related Devices (Code: FSH)

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.

K884876S 4 INSTRUMENT STANDCarl Zeiss, Inc.K821921STAND, SURG. INSTRUMENT & DRESSINGEmerson-Sack-Warner Corp.K813337SKINNY CHIBA NEEDLE & TRAYAmerican Pharmaseal Div. AhscK813338BIOPSY NEEDLES & TRAYSAmerican Pharmaseal Div. AhscK813335PERCUTANEOUS TRANSHEPATIC CHOLANG. TRAYAmerican Pharmaseal Div. AhscK780759MODEL 902 STANDApplied Medical Research

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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