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FDA 510(k)

WALL MOUNTED LASER POSITIONING DEVICE

K-Number: K801541 · 1980-08-20

ApplicantAdvantage Medical Systems, Inc.
Decision Date1980-08-20
Product CodeIWE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WALL MOUNTED LASER POSITIONING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Advantage Medical Systems, Inc.. It received FDA 510(k) clearance on 1980-08-20 under 510(k) number K801541. The device is classified under product code IWE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALL MOUNTED LASER POSITIONING DEVICE?

WALL MOUNTED LASER POSITIONING DEVICE is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Advantage Medical Systems, Inc.. The 510(k) number is K801541.

When did WALL MOUNTED LASER POSITIONING DEVICE receive FDA 510(k) clearance?

WALL MOUNTED LASER POSITIONING DEVICE received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801541.

Who is the listed applicant for WALL MOUNTED LASER POSITIONING DEVICE?

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

What is the FDA product code for WALL MOUNTED LASER POSITIONING DEVICE?

The FDA product code for WALL MOUNTED LASER POSITIONING DEVICE is IWE.

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Other records listing Advantage Medical Systems, 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.

K873957NON-CORING HUBER TYPE NEEDLESK873290LACERATION AND INSTRUMENT TRAYSK863494NEONATAL PHYSIOLOGICAL MONITOR MODEL PM 20K861556MODIFIED FETAL MONITOR MODEL FM-2K861279FLUORO PLUSK861455MODEL DT-102 DATA TELEPHONE TRANSMITTER

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Related Devices (Code: IWE)

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.

K973162DUAL RADIATION TARGETING SYSTEM DRTS DRAPEHogan & HartsonK955236GREEN TEC-2100Medtec, Inc.K954414CENTRALITE BACKPOINTERDiacor, Inc.K950293TEC-2110 GREEN LASER MODEL MT-HNGMedtec, Inc.K950112CENTRALITE(R)-DLL SERIESDiacor, Inc.K951601MED-TEC STRING RETICLE TRAYMedtec, 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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