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FDA 510(k)

INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER

K-Number: K971950 · 1997-08-01

ApplicantInfinitech, Inc.
Decision Date1997-08-01
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Infinitech, Inc.. It received FDA 510(k) clearance on 1997-08-01 under 510(k) number K971950. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER?

INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER is a medical device that received FDA 510(k) clearance on 1997-08-01. The listed applicant is Infinitech, Inc.. The 510(k) number is K971950.

When did INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER receive FDA 510(k) clearance?

INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER received FDA 510(k) clearance on 1997-08-01, under 510(k) number K971950.

Who is the listed applicant for INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER?

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

What is the FDA product code for INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER?

The FDA product code for INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER is HQF.

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Other records listing Infinitech, 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.

K972506INFINITECH BULLET ENDO ILLUMINATED PICK MANIPULATORK951627INFINITECH HIGH INTENSITY XENON LIGHT SOURCE SYSTEMK931264INFINITECH OTOPROBEK931546END-IRRIGATING ENDOILLUMINATORK935441INFINITECH BREATH EZ

Related Devices (Code: HQF)

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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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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