510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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REPNot classified

Surveying Laser Product

Unknown
FDA source (opens on fda.gov)

REP is the FDA product code for Surveying Laser Product. FDA's definition for this code reads: "Product, laser, surveying, instrument, determine position by measurement of angles". As of , FDA records hold no 510(k) clearances under this code and 4 recalls.

Classification record

Product code
REP
Device name
Surveying Laser Product
FDA definition
Product, laser, surveying, instrument, determine position by measurement of angles
Device class
Not classified
Review panel
Unknown
Submission type
FDA code null
GMP exempt
Yes
Ingested clearances
0
Ingested recalls
4

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code REP.