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FDA 510(k)

RGB CAMERA SYSTEM

K-Number: K872661 · 1987-07-21

ApplicantAspen Laboratories, Inc.
Decision Date1987-07-21
Product CodeFWF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RGB CAMERA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1987-07-21 under 510(k) number K872661. The device is classified under product code FWF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RGB CAMERA SYSTEM?

RGB CAMERA SYSTEM is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K872661.

When did RGB CAMERA SYSTEM receive FDA 510(k) clearance?

RGB CAMERA SYSTEM received FDA 510(k) clearance on 1987-07-21, under 510(k) number K872661.

Who is the listed applicant for RGB CAMERA SYSTEM?

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

What is the FDA product code for RGB CAMERA SYSTEM?

The FDA product code for RGB CAMERA SYSTEM is FWF.

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Other records listing Aspen Laboratories, 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.

K981220SYSTEM 7500 ABC ELECTROSURGICAL UNITK963088SHEATH, ELECTROSURGICAL PENCILK955834SYSTEM 6500 ABC ELECTROSURGICAL UNITK9602964000 ETMK953081BEAMER PLUSK953007EXCALIBUR PLUS ELECTROSURGICAL UNIT

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Related Devices (Code: FWF)

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.

K053412FLEXISCOPE, MODELS 50MH AND 50 MHCSchoelly Imaging, Inc.K990154KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEMKarl Storz Imaging, Inc.K982754EC-1000-7 DIGITAL ENDOSCOPY VIDEO CAMERA, MODELS EC 1000-7P (PAL) & EC 1000-7N (NTSC)A.Stein - Regulatory Affairs ConsultingK982965ENDOCAM CAMERA SYSTEMS 5502/5507 WITH CR CAMERA HEADS AND ACCESSORIESRichard Wolf Medical Instruments Corp.K982397VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEMAngiolaz, Inc.K982409VES 1501-MAngiolaz, 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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