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FDA 510(k)

CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE

K-Number: K864610 · 1987-06-18

ApplicantInframed, Inc.
Decision Date1987-06-18
Product CodeLLF
DecisionSubstantially Equivalent

Device Summary

CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE is the device name listed in this FDA 510(k) record. The listed applicant is Inframed, Inc.. It received FDA 510(k) clearance on 1987-06-18 under 510(k) number K864610. The device is classified under product code LLF. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE?

CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE is a medical device that received FDA 510(k) clearance on 1987-06-18. The listed applicant is Inframed, Inc.. The 510(k) number is K864610.

When did CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE receive FDA 510(k) clearance?

CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE received FDA 510(k) clearance on 1987-06-18, under 510(k) number K864610.

Who is the listed applicant for CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE?

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

What is the FDA product code for CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE?

The FDA product code for CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE is LLF.

Related Clinical Trials

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Other records listing Inframed, 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.

K852761CILAS MODEL YM101K844178MODEL TT25RF

Related Devices (Code: LLF)

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.

K870773ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASERHgm, Inc.K860977MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATIONBritt Corp., Inc.K833497COOPER MEDICAL MODEL 770Cooper Medical Corp.

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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