510(k) K833211
K833211 is an FDA 510(k) premarket notification submitted by Acumedia Manufacturers, Inc. for the device "BILE SALTS MIXTURE". The FDA issued a decision of Substantially Equivalent on October 27, 1983. The device falls under product code JKS (Spectral Absorb. Curve, Oxyhemoglobin, Carboxyhemoglobin, Carbon-Monoxide), a Class I device regulated under 21 CFR 862.3220. Acumedia Manufacturers, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 27, 1983
- Date Received
- September 19, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Spectral Absorb. Curve, Oxyhemoglobin, Carboxyhemoglobin, Carbon-Monoxide
- Device Class
- Class I
- Regulation Number
- 862.3220
- Review Panel
- TX
- Submission Type