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FDA 510(k)

MODEL 300GE1500 SHOULDER COIL

K-Number: K933658 · 1993-11-19

ApplicantMedic, Inc.
Decision Date1993-11-19
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 300GE1500 SHOULDER COIL is the device name listed in this FDA 510(k) record. The listed applicant is Medic, Inc.. It received FDA 510(k) clearance on 1993-11-19 under 510(k) number K933658. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 300GE1500 SHOULDER COIL?

MODEL 300GE1500 SHOULDER COIL is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is Medic, Inc.. The 510(k) number is K933658.

When did MODEL 300GE1500 SHOULDER COIL receive FDA 510(k) clearance?

MODEL 300GE1500 SHOULDER COIL received FDA 510(k) clearance on 1993-11-19, under 510(k) number K933658.

Who is the listed applicant for MODEL 300GE1500 SHOULDER COIL?

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

What is the FDA product code for MODEL 300GE1500 SHOULDER COIL?

The FDA product code for MODEL 300GE1500 SHOULDER COIL is LNH.

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Other records listing Medic, 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.

K0223951.5T SCANMED PV ARRAYK951649MODEL #801GE1500 PEDIATRIC ARRAY COILK942874MODEL #300TO3500 SHOULDER COILK942875MODEL #900TO3500 HEAD/NECK COILK942873MODEL #700TO3500 NECK/ABDOMINAL COILK942355MODEL #310T03500 WRIST COIL

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Related Devices (Code: LNH)

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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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