The following data is part of a premarket notification filed by R & D Batteries, Inc. with the FDA for R&d Battries, Inc. Part Numbers 5601, 5602, 5624 And 5626.
Device ID | K951274 |
510k Number | K951274 |
Device Name: | R&D BATTRIES, INC. PART NUMBERS 5601, 5602, 5624 AND 5626 |
Classification | Thermometer, Electronic, Clinical |
Applicant | R & D BATTERIES, INC. 400 GATEWAY BLVD. Burnsville, MN 55337 |
Contact | Randall C Noddings |
Correspondent | Randall C Noddings R & D BATTERIES, INC. 400 GATEWAY BLVD. Burnsville, MN 55337 |
Product Code | FLL |
CFR Regulation Number | 880.2910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-03-21 |
Decision Date | 1995-08-18 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00810149093401 | K951274 | 000 |
00810149091469 | K951274 | 000 |
00810149091476 | K951274 | 000 |
00810149091612 | K951274 | 000 |
00810149091674 | K951274 | 000 |
00810149092275 | K951274 | 000 |
00810149092336 | K951274 | 000 |
00810149092343 | K951274 | 000 |
00810149092497 | K951274 | 000 |
00810149092503 | K951274 | 000 |
00810149092718 | K951274 | 000 |
00810149090899 | K951274 | 000 |