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FDA 510(k)

SERVICE MASTER (IMPULSE)

K-Number: K873300 · 1987-12-08

ApplicantRichards Medical Co., Inc.
Decision Date1987-12-08
Product CodeLRB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SERVICE MASTER (IMPULSE) 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 1987-12-08 under 510(k) number K873300. The device is classified under product code LRB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVICE MASTER (IMPULSE)?

SERVICE MASTER (IMPULSE) is a medical device that received FDA 510(k) clearance on 1987-12-08. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K873300.

When did SERVICE MASTER (IMPULSE) receive FDA 510(k) clearance?

SERVICE MASTER (IMPULSE) received FDA 510(k) clearance on 1987-12-08, under 510(k) number K873300.

Who is the listed applicant for SERVICE MASTER (IMPULSE)?

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 SERVICE MASTER (IMPULSE)?

The FDA product code for SERVICE MASTER (IMPULSE) is LRB.

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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

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Related Devices (Code: LRB)

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.

K974219FACEPLATE ASSEMBLYFinetone Hearing InstrumentsK961593INTRASTAR PRE-WIRED FACEPLATE FOR IN-THE-EAR HEARING AIDSSegi Hearing Aid Co.K942722MODULE PROGRAMElectone, Inc.K942236AUDINA PREWIRES (FACEPLATE HEARING AID SERIES)Audina Hearing InstrumentK935048ARTISAN PROGRAMMER & HEARING AIDTelex Communications, Inc.K933045SILVER RECHARGEABLE MODULE, ITEElectone, Inc.

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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