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FDA 510(k)

MODEL MC-1 SURGICAL VIDEO CAMERA

K-Number: K863376 · 1986-10-02

ApplicantBiometric Products, Inc.
Decision Date1986-10-02
Product CodeFWF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL MC-1 SURGICAL VIDEO CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Biometric Products, Inc.. It received FDA 510(k) clearance on 1986-10-02 under 510(k) number K863376. 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 MODEL MC-1 SURGICAL VIDEO CAMERA?

MODEL MC-1 SURGICAL VIDEO CAMERA is a medical device that received FDA 510(k) clearance on 1986-10-02. The listed applicant is Biometric Products, Inc.. The 510(k) number is K863376.

When did MODEL MC-1 SURGICAL VIDEO CAMERA receive FDA 510(k) clearance?

MODEL MC-1 SURGICAL VIDEO CAMERA received FDA 510(k) clearance on 1986-10-02, under 510(k) number K863376.

Who is the listed applicant for MODEL MC-1 SURGICAL VIDEO CAMERA?

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

What is the FDA product code for MODEL MC-1 SURGICAL VIDEO CAMERA?

The FDA product code for MODEL MC-1 SURGICAL VIDEO CAMERA is FWF.

Related Clinical Trials

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.

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Other records listing Biometric Products, 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.

K933021MODEL T131 MEMORY TRANSMITTERK842435MODEL T 101 CLINICAL TRANSMITTERK840032TELEPHONE RECEIVERS R101 R111K832951MEMORY LOOP TRANSMITTER #121

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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