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FDA 510(k)

MINOR SURGERY LIGHT MODEL 2112

K-Number: K860020 · 1986-01-24

ApplicantAdel Medical , Ltd.
Decision Date1986-01-24
Product CodeFSS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINOR SURGERY LIGHT MODEL 2112 is the device name listed in this FDA 510(k) record. The listed applicant is Adel Medical , Ltd.. It received FDA 510(k) clearance on 1986-01-24 under 510(k) number K860020. The device is classified under product code FSS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINOR SURGERY LIGHT MODEL 2112?

MINOR SURGERY LIGHT MODEL 2112 is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Adel Medical , Ltd.. The 510(k) number is K860020.

When did MINOR SURGERY LIGHT MODEL 2112 receive FDA 510(k) clearance?

MINOR SURGERY LIGHT MODEL 2112 received FDA 510(k) clearance on 1986-01-24, under 510(k) number K860020.

Who is the listed applicant for MINOR SURGERY LIGHT MODEL 2112?

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

What is the FDA product code for MINOR SURGERY LIGHT MODEL 2112?

The FDA product code for MINOR SURGERY LIGHT MODEL 2112 is FSS.

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Other records listing Adel Medical , Ltd. 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.

K890476ADEL - MODEL 986 INFANT WARMERK874610ADEL MODEL 2100 BIRTHING BEDK871475SOLOLIFT - PATIENT TRANSFER STRETCHERK861030LABOR-DELIVERY STRETCH/BEDK833321LABOR/DELIVERY/RECOVERY BED LDR-600K810886ADEL MEDICAL BIRTHING BED, #LD-500

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Related Devices (Code: FSS)

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.

K091246ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M)Trumpf Medizin Systeme GmbH + Co. KGK003489NEXT GENERAL M20 SURGICAL LIGHT; NEXT GENERATION M16 MINOR SURGERY LIGHT; NEXT GENERATION SPOTLIGHT; NEXT GENERATION M8Medical Illumination International, Inc.K984124AESCULAP XENON LIGHT SOURCEAesculap, Inc.K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCECuda Products Co.K981821VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATORAngiolaz, Inc.K981469CERMAX300 LIGHTSOURCECuda Products Co.

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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