ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP
K-Number: K864608 · 1986-12-16
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Device Summary
Frequently Asked Questions
What is the ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP?
ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP is a medical device that received FDA 510(k) clearance on 1986-12-16. The listed applicant is Adobe Ent.. The 510(k) number is K864608.
When did ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP receive FDA 510(k) clearance?
ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP received FDA 510(k) clearance on 1986-12-16, under 510(k) number K864608.
Who is the listed applicant for ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP?
The FDA 510(k) record lists Adobe Ent. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP?
The FDA product code for ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP is GEN.
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.
Related Devices (Code: GEN)
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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