Atlas FDA

PALAVIT GLC

FDA 510(k) clearance K904928 · decided 1991-06-06

Clearance details

K-number
K904928
Device name
PALAVIT GLC
Applicant
Kulzer, Inc.
Decision
Substantially Equivalent
Date received
1990-10-31
Decision date
1991-06-06
Days to decision
218 days
Clearance type
Traditional
Product code
EGD
Device class
1
Regulation number
872.6890
Medical specialty
Dental
Advisory committee
Dental
Location
Irvine, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
BRACE EZE (K020009)Udent, Inc.2002-02-11
GLENROE ORTHO-SIL (K945535)Glenroe Technologies1995-01-27
ORTHO WAX (K924024)Heraeus Kulzer, Inc.1992-11-17
BURNOUT MATERIAL (K923586)Dentsply Intl.1992-09-29
SALIVA-STIM (K914892)Orion Diagnostica, Inc.1992-09-02
BITE RIM WAX (K922380)Dentsply Intl.1992-06-16
PALAVIT G (K914513)Heraeus Kulzer, Inc.1992-03-19
INTRAORAL DENTAL WAX (K910676)Pemaco, Inc.1991-08-21
PEMACO 2000 INTRAORAL DENTAL WAX (K895562)Pemaco, Inc.1989-11-06
PEMACO 3000 INTRAORAL DENTAL WAX (K895561)Pemaco, Inc.1989-11-06
PEMACO BITE WAX SHEETS (K895563)Pemaco, Inc.1989-11-06
PEMACO ECONOMY BASE PLATE WAX-MEDIUM SOFT (K895566)Pemaco, Inc.1989-11-06

Recalls involving this device

No recalls on record reference this clearance.