BACH-SIMPSON MODEL BVM30
K-Number: K811615 · 1981-08-13
Device Summary
Frequently Asked Questions
What is the BACH-SIMPSON MODEL BVM30?
BACH-SIMPSON MODEL BVM30 is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Bach-Simpson , Ltd.. The 510(k) number is K811615.
When did BACH-SIMPSON MODEL BVM30 receive FDA 510(k) clearance?
BACH-SIMPSON MODEL BVM30 received FDA 510(k) clearance on 1981-08-13, under 510(k) number K811615.
Who is the listed applicant for BACH-SIMPSON MODEL BVM30?
The FDA 510(k) record lists Bach-Simpson , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BACH-SIMPSON MODEL BVM30?
The FDA product code for BACH-SIMPSON MODEL BVM30 is DPW.
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 Bach-Simpson , Ltd. 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: DPW)
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.