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FDA 510(k)

PURITAS 100% COTTON ABSORB OPER ROOM SURG TOWELS

K-Number: K912542 · 1991-07-23

ApplicantPuritas Health Care, Inc.
Decision Date1991-07-23
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PURITAS 100% COTTON ABSORB OPER ROOM SURG TOWELS is the device name listed in this FDA 510(k) record. The listed applicant is Puritas Health Care, Inc.. It received FDA 510(k) clearance on 1991-07-23 under 510(k) number K912542. 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 PURITAS 100% COTTON ABSORB OPER ROOM SURG TOWELS?

PURITAS 100% COTTON ABSORB OPER ROOM SURG TOWELS is a medical device that received FDA 510(k) clearance on 1991-07-23. The listed applicant is Puritas Health Care, Inc.. The 510(k) number is K912542.

When did PURITAS 100% COTTON ABSORB OPER ROOM SURG TOWELS receive FDA 510(k) clearance?

PURITAS 100% COTTON ABSORB OPER ROOM SURG TOWELS received FDA 510(k) clearance on 1991-07-23, under 510(k) number K912542.

Who is the listed applicant for PURITAS 100% COTTON ABSORB OPER ROOM SURG TOWELS?

The FDA 510(k) record lists Puritas Health Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PURITAS 100% COTTON ABSORB OPER ROOM SURG TOWELS?

The FDA product code for PURITAS 100% COTTON ABSORB OPER ROOM SURG TOWELS is KKX.

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Other records listing Puritas Health Care, 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.

K942339SKIN NEUVEAU SCAR TREATMENTK941197SILK*SKIN SCAR TREATMENTK935600TRACHEAL SUCTION CATHETERK935531OP-FLEX SUMP SUCTION SET WITH DIFFUSER TIPK940074Y-TYPE BLOOD ADMINISTRATION SETK940055MULTISET

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Related Devices (Code: KKX)

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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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