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FDA 510(k)

AQUACEL SURGICAL PREP PADS

K-Number: K861937 · 1986-06-06

ApplicantAdvanced Ortho-Technology, Inc.
Decision Date1986-06-06
Product Code
DecisionSubstantially Equivalent

Device Summary

AQUACEL SURGICAL PREP PADS is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Ortho-Technology, Inc.. It received FDA 510(k) clearance on 1986-06-06 under 510(k) number K861937. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUACEL SURGICAL PREP PADS?

AQUACEL SURGICAL PREP PADS is a medical device that received FDA 510(k) clearance on 1986-06-06. The listed applicant is Advanced Ortho-Technology, Inc.. The 510(k) number is K861937.

When did AQUACEL SURGICAL PREP PADS receive FDA 510(k) clearance?

AQUACEL SURGICAL PREP PADS received FDA 510(k) clearance on 1986-06-06, under 510(k) number K861937.

Who is the listed applicant for AQUACEL SURGICAL PREP PADS?

The FDA 510(k) record lists Advanced Ortho-Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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Other records listing Advanced Ortho-Technology, 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.

K854241AOT EXTERNAL COMPRESS DEVICEK854344AQUACEL SURGICAL PREP PADS

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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