CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER
K-Number: K901677 · 1990-04-23
Advertisement
Device Summary
Frequently Asked Questions
What is the CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER?
CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER is a medical device that received FDA 510(k) clearance on 1990-04-23. The listed applicant is Buckman Co., Inc.. The 510(k) number is K901677.
When did CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER receive FDA 510(k) clearance?
CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER received FDA 510(k) clearance on 1990-04-23, under 510(k) number K901677.
Who is the listed applicant for CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER?
The FDA 510(k) record lists Buckman Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER?
The FDA product code for CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER is LGH.
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 Buckman 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: LGH)
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