CASPAR SCALP CLIP, APPLIER
K-Number: K890443 · 1989-06-15
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Device Summary
Frequently Asked Questions
What is the CASPAR SCALP CLIP, APPLIER?
CASPAR SCALP CLIP, APPLIER is a medical device that received FDA 510(k) clearance on 1989-06-15. The listed applicant is Aesculap Instruments Corp.. The 510(k) number is K890443.
When did CASPAR SCALP CLIP, APPLIER receive FDA 510(k) clearance?
CASPAR SCALP CLIP, APPLIER received FDA 510(k) clearance on 1989-06-15, under 510(k) number K890443.
Who is the listed applicant for CASPAR SCALP CLIP, APPLIER?
The FDA 510(k) record lists Aesculap Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CASPAR SCALP CLIP, APPLIER?
The FDA product code for CASPAR SCALP CLIP, APPLIER is HBO.
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 Aesculap Instruments Corp. 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: HBO)
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.
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