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FDA 510(k)

INTEROOM(POWERED OPHTHALMIC TABLE)

K-Number: K803176 · 1981-01-09

ApplicantJocevest Interoom, Inc.
Decision Date1981-01-09
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTEROOM(POWERED OPHTHALMIC TABLE) is the device name listed in this FDA 510(k) record. The listed applicant is Jocevest Interoom, Inc.. It received FDA 510(k) clearance on 1981-01-09 under 510(k) number K803176. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEROOM(POWERED OPHTHALMIC TABLE)?

INTEROOM(POWERED OPHTHALMIC TABLE) is a medical device that received FDA 510(k) clearance on 1981-01-09. The listed applicant is Jocevest Interoom, Inc.. The 510(k) number is K803176.

When did INTEROOM(POWERED OPHTHALMIC TABLE) receive FDA 510(k) clearance?

INTEROOM(POWERED OPHTHALMIC TABLE) received FDA 510(k) clearance on 1981-01-09, under 510(k) number K803176.

Who is the listed applicant for INTEROOM(POWERED OPHTHALMIC TABLE)?

The FDA 510(k) record lists Jocevest Interoom, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTEROOM(POWERED OPHTHALMIC TABLE)?

The FDA product code for INTEROOM(POWERED OPHTHALMIC TABLE) is HRS.

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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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