510(k) K800971
K800971 is an FDA 510(k) premarket notification submitted by Mr Associates, Inc. for the device "M.R. ASSOC. MAGNETIC EXTRACTOR". The FDA issued a decision of Substantially Equivalent on May 8, 1980. The device falls under product code FCC (Endoscopic Magnetic Retriever), a Class II device regulated under 21 CFR 876.1500. Mr Associates, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 8, 1980
- Date Received
- April 23, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Endoscopic Magnetic Retriever
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type
to endoscopically retrieve magnetic foreign objects