510(k) K831387
K831387 is an FDA 510(k) premarket notification submitted by The Perkin-Elmer Corp. for the device "HS-100 HEADSPACE SAMPLING ACCESSORY". The FDA issued a decision of Substantially Equivalent on August 24, 1983. The device falls under product code KZQ (Chromatography(Gas), Clinical Use), a Class I device regulated under 21 CFR 862.2250. The Perkin-Elmer Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 24, 1983
- Date Received
- April 28, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Chromatography(Gas), Clinical Use
- Device Class
- Class I
- Regulation Number
- 862.2250
- Review Panel
- TX
- Submission Type