The following data is part of a premarket notification filed by Sps Medical Supply Corp. with the FDA for Label, Sterilization Indicator; Dual Steam/e.o.gas.
Device ID | K890763 |
510k Number | K890763 |
Device Name: | LABEL, STERILIZATION INDICATOR; DUAL STEAM/E.O.GAS |
Classification | Indicator, Physical/chemical Sterilization Process |
Applicant | SPS MEDICAL SUPPLY CORP. 1250 SCOTTSVILLE RD. Rochester, NY 14624 |
Contact | Jack Scoville |
Correspondent | Jack Scoville SPS MEDICAL SUPPLY CORP. 1250 SCOTTSVILLE RD. Rochester, NY 14624 |
Product Code | JOJ |
CFR Regulation Number | 880.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-02-14 |
Decision Date | 1989-08-07 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
50732224750755 | K890763 | 000 |
50732224730719 | K890763 | 000 |
50732224730696 | K890763 | 000 |
50732224710070 | K890763 | 000 |