510(k) K772377
K772377 is an FDA 510(k) premarket notification submitted by Edward Weck, Inc. for the device "HILDYARD POST NASAL FORCEP". The FDA issued a decision of Substantially Equivalent on January 17, 1978. The device falls under product code KAE (Forceps, Ent), a Class I device regulated under 21 CFR 874.4420. Edward Weck, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 17, 1978
- Date Received
- December 27, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Forceps, Ent
- Device Class
- Class I
- Regulation Number
- 874.4420
- Review Panel
- EN
- Submission Type