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FDA 510(k)

RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT

K-Number: K882244 · 1988-06-23

ApplicantRichards Medical Co., Inc.
Decision Date1988-06-23
Product CodeEPP
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1988-06-23 under 510(k) number K882244. The device is classified under product code EPP. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT?

RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT is a medical device that received FDA 510(k) clearance on 1988-06-23. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K882244.

When did RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT receive FDA 510(k) clearance?

RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT received FDA 510(k) clearance on 1988-06-23, under 510(k) number K882244.

Who is the listed applicant for RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT?

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

What is the FDA product code for RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT?

The FDA product code for RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT is EPP.

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Other records listing Richards Medical Co., 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.

K896106ROGOZINSKI SPINAL SYSTEM, ADD'L COMPONENTSK900628MODULAR HIP SYSTEMK896580UNI-POLAR HEADK895241INTRAMEDULLARY HIP SCREWK884824TRICON-M TOTAL KNEE SYSTEMK896204ZIRCONIA CERAMIC HEAD ADD'L SIZES

View all 71 devices →

Related Devices (Code: EPP)

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.

K942158AQUAPLAST NASAL SPLINTS, PRECUT SILVER SPLINT PATTERNS AND SPLINT KITSWfr/Aquaplast Corp.K942724EXTERNAL NASAL SPLINTMicromed Development Corp.K895502MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINTMicrobio-Medics, Inc.K890599HOOD NASAL SPLINTHood LaboratoriesK872905AMERICAN NASAL SPONGEAmerican Silk Sutures, Inc.K864932'EXMOOR' CAWOOD NASAL SPLINTSExmoor Plastics , Ltd.

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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