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FDA 510(k)

SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269

K-Number: K871368 · 1987-05-01

ApplicantSchell B.V.
Decision Date1987-05-01
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269 is the device name listed in this FDA 510(k) record. The listed applicant is Schell B.V.. It received FDA 510(k) clearance on 1987-05-01 under 510(k) number K871368. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269?

SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269 is a medical device that received FDA 510(k) clearance on 1987-05-01. The listed applicant is Schell B.V.. The 510(k) number is K871368.

When did SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269 receive FDA 510(k) clearance?

SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269 received FDA 510(k) clearance on 1987-05-01, under 510(k) number K871368.

Who is the listed applicant for SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269?

The FDA 510(k) record lists Schell B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269?

The FDA product code for SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269 is IOQ.

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Related Devices (Code: IOQ)

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.

K122473TOTALCARE SPOT TOTALCARE BARIATRIC TOTALCARE DUO TOATALCARE BED SYSTEM TOTALCARE DUO2Hill-RomK973624NURSE'S AID PATIENT ROTATION SYSTEMAir Med Assist ProductsK970364AIRTEC2 LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970363HYDROTEC LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970636TOTALCARE., MODULAR THERAPY SYSTEM (MTS)Hill-Rom, Inc.K964873SILKAIR LOW AIRLOSS THERAPYHill-Rom, Inc.

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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