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FDA 510(k)

MOBILE OPERATING TABLE FOR ORL MICROSURGERY

K-Number: K853720 · 1985-10-18

Decision Date1985-10-18
Product CodeGDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MOBILE OPERATING TABLE FOR ORL MICROSURGERY 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 1985-10-18 under 510(k) number K853720. The device is classified under product code GDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBILE OPERATING TABLE FOR ORL MICROSURGERY?

MOBILE OPERATING TABLE FOR ORL MICROSURGERY is a medical device that received FDA 510(k) clearance on 1985-10-18. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K853720.

When did MOBILE OPERATING TABLE FOR ORL MICROSURGERY receive FDA 510(k) clearance?

MOBILE OPERATING TABLE FOR ORL MICROSURGERY received FDA 510(k) clearance on 1985-10-18, under 510(k) number K853720.

Who is the listed applicant for MOBILE OPERATING TABLE FOR ORL MICROSURGERY?

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 MOBILE OPERATING TABLE FOR ORL MICROSURGERY?

The FDA product code for MOBILE OPERATING TABLE FOR ORL MICROSURGERY is GDC.

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.

View all 44 devices →

Related Devices (Code: GDC)

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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