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FDA 510(k)

CONVERTORS OPTI-SORB DRAPE MATERIAL

K-Number: K940702 · 1994-04-26

Decision Date1994-04-26
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONVERTORS OPTI-SORB DRAPE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1994-04-26 under 510(k) number K940702. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVERTORS OPTI-SORB DRAPE MATERIAL?

CONVERTORS OPTI-SORB DRAPE MATERIAL is a medical device that received FDA 510(k) clearance on 1994-04-26. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K940702.

When did CONVERTORS OPTI-SORB DRAPE MATERIAL receive FDA 510(k) clearance?

CONVERTORS OPTI-SORB DRAPE MATERIAL received FDA 510(k) clearance on 1994-04-26, under 510(k) number K940702.

Who is the listed applicant for CONVERTORS OPTI-SORB DRAPE MATERIAL?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVERTORS OPTI-SORB DRAPE MATERIAL?

The FDA product code for CONVERTORS OPTI-SORB DRAPE MATERIAL is KKX.

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 Baxter Healthcare 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.

View all 504 devices →

Related Devices (Code: KKX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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