Company ยท US
Health Products, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 1992. Name variants (Inc, Corp, punctuation) are merged.
13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| BWF | Spirometer, Therapeutic (Incentive) | 4 |
| BZH | Meter, Peak Flow, Spirometry | 3 |
| CAF | Nebulizer (Direct Patient Interface) | 1 |
| FNL | Bed, Ac-Powered Adjustable Hospital | 1 |
| FNM | Mattress, Air Flotation, Alternating Pressure | 1 |
| INO | Chair, Positioning, Electric | 1 |
| IOQ | Bed, Flotation Therapy, Powered | 1 |
| KQX | Goniometer, Ac-Powered | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 13, 1992 | K912866 | PEAK EXPIRATORY FLOW METER Health Products, Inc. | BZH |
| Jan 30, 1992 | K912943 | THRESHOLD 2X INSPIRATORY MUSCLE TRAINER Health Products, Inc. | BWF |
| Oct 23, 1991 | K911807 | METERED DOSE INHALER (MDI) SPACER Health Products, Inc. | CAF |
| Aug 10, 1990 | K902292 | MODIFIED ASSESS(R) PEAK FLOW METER Health Products, Inc. | BZH |
| Jan 30, 1990 | K896953 | MODIFIED ASSESS(R) PEAK FLOW METER Health Products, Inc. | BZH |
| Aug 9, 1989 | K894353 | ORTHODERM CONVERTIBLE Health Products, Inc. | IOQ |
| Apr 5, 1989 | K890426 | CONSUMMATE AIR THERAPY BED Health Products, Inc. | FNL |
| Feb 5, 1988 | K874801 | ORTHODERM THERAPY BED Health Products, Inc. | FNM |
| Jun 15, 1987 | K871742 | MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER Health Products, Inc. | BWF |
| Mar 31, 1987 | K870514 | THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER Health Products, Inc. | BWF |
| Mar 16, 1987 | K864719 | PFLEX EM(TM) (EXERCISE MONITOR) Health Products, Inc. | BWF |
| Dec 24, 1986 | K864918 | HEALTH PRODUCTS, INC. ORTHODERM THERAPY CHAIR Health Products, Inc. | INO |
| Jul 11, 1986 | K862128 | DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER) Health Products, Inc. | KQX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||