THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM
K-Number: K931594 · 1993-12-21
Advertisement
Device Summary
Frequently Asked Questions
What is the THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM?
THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM is a medical device that received FDA 510(k) clearance on 1993-12-21. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K931594.
When did THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM receive FDA 510(k) clearance?
THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM received FDA 510(k) clearance on 1993-12-21, under 510(k) number K931594.
Who is the listed applicant for THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM?
The FDA 510(k) record lists Medical Device Inspection Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM?
The FDA product code for THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM is IOQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Medical Device Inspection Co., Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IOQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement