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FDA 510(k)

SURGICAL HEAD DRAPE, DISP.

K-Number: K771136 · 1977-07-14

Decision Date1977-07-14
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL HEAD DRAPE, DISP. is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Mfg. Co.. It received FDA 510(k) clearance on 1977-07-14 under 510(k) number K771136. 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 SURGICAL HEAD DRAPE, DISP.?

SURGICAL HEAD DRAPE, DISP. is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K771136.

When did SURGICAL HEAD DRAPE, DISP. receive FDA 510(k) clearance?

SURGICAL HEAD DRAPE, DISP. received FDA 510(k) clearance on 1977-07-14, under 510(k) number K771136.

Who is the listed applicant for SURGICAL HEAD DRAPE, DISP.?

The FDA 510(k) record lists Procter & Gamble Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL HEAD DRAPE, DISP.?

The FDA product code for SURGICAL HEAD DRAPE, DISP. 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 Procter & Gamble Mfg. Co. 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 72 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

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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